Friday, September 30, 2016

Protegra


Pronunciation: MUL-ti-VYE-ta-mins/MIN-er-als
Generic Name: Multivitamins with Minerals
Brand Name: Examples include Protegra and Vicon Forte


Protegra is used for:

Treating or preventing low levels of vitamins and minerals in the body. It may also be used for other conditions as determined by your doctor.


Protegra is a vitamin and mineral supplement. It works by providing extra vitamins and minerals to the body.


Do NOT use Protegra if:


  • you are allergic to any ingredient in Protegra

Contact your doctor or health care provider right away if any of these apply to you.



Before using Protegra:


Some medical conditions may interact with Protegra. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

Some MEDICINES MAY INTERACT with Protegra.


Ask your health care provider if Protegra may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Protegra:


Use Protegra as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Protegra by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

  • If you miss a dose of Protegra, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Protegra.



Important safety information:


  • Do not take large doses of vitamins while you use Protegra unless your doctor tells you to.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Protegra while you are pregnant. It is not known if Protegra is found in breast milk. If you are or will be breast-feeding while you use Protegra, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Protegra:


All medicines may cause side effects, but many people have no, or minor, side effects. No COMMON side effects have been reported with Protegra. Seek medical attention right away if any of these SEVERE side effects occur:



Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.



If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include nausea; vomiting.


Proper storage of Protegra:

Store Protegra at room temperature. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Protegra out of the reach of children and away from pets.


General information:


  • If you have any questions about Protegra, please talk with your doctor, pharmacist, or other health care provider.

  • Protegra is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Protegra. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Protegra resources


  • Protegra Use in Pregnancy & Breastfeeding
  • Protegra Drug Interactions
  • Protegra Support Group
  • 4 Reviews for Protegra - Add your own review/rating


  • multivitamin Concise Consumer Information (Cerner Multum)

  • Folplex Prescribing Information (FDA)

  • Foltabs 800 Prescribing Information (FDA)

  • Infuvite Pediatric Prescribing Information (FDA)

  • Nephrocaps Prescribing Information (FDA)

  • Nephrocaps

  • Renal Caps Prescribing Information (FDA)

  • Vitamin A Monograph (AHFS DI)



Compare Protegra with other medications


  • Vitamin/Mineral Supplementation and Deficiency

Thiogule




Thiogule may be available in the countries listed below.


Ingredient matches for Thiogule



Carteolol

Carteolol hydrochloride (a derivative of Carteolol) is reported as an ingredient of Thiogule in the following countries:


  • Japan

International Drug Name Search

Miristalkonium Chloride




Scheme

Rec.INN

CAS registry number (Chemical Abstracts Service)

0000139-08-2

Chemical Formula

C23-H42-Cl-N

Molecular Weight

368

Therapeutic Categories

Antiseptic

Disinfectant

Contraceptive, spermicidal agent

Chemical Name

Benzenemethanaminium, N,N-dimethyl-N-tetradecyl-, chloride

Foreign Names

  • Miristalkonii Chloridum (Latin)
  • Miristalkonium chlorid (German)
  • Chlorure de Miristalkonium (French)
  • Cloruro de miristalconio (Spanish)

Generic Names

  • Miristalkonium Chloride (OS: BAN)
  • Miristylbenzalkonium chloride (IS)

Brand Name

  • Alpagelle
    CAG, France

International Drug Name Search

Glossary

BANBritish Approved Name
ISInofficial Synonym
OSOfficial Synonym
Rec.INNRecommended International Nonproprietary Name (World Health Organization)

Click for further information on drug naming conventions and International Nonproprietary Names.

Propranolol-CT




Propranolol-CT may be available in the countries listed below.


Ingredient matches for Propranolol-CT



Propranolol

Propranolol hydrochloride (a derivative of Propranolol) is reported as an ingredient of Propranolol-CT in the following countries:


  • Germany

International Drug Name Search

Atovaquone and Proguanil Hydrochloride


Class: Antimalarials
Chemical Name: trans-2-[4-(4-Chlorophenyl)cyclohexyl]-3-hydroxy-1,4-naphthalenedione
CAS Number: 95233-18-4
Brands: Malarone

Introduction

Antimalarial; fixed combination containing 2 antimalarials (atovaquone, proguanil).1


Uses for Atovaquone and Proguanil Hydrochloride


Malaria


Prevention (prophylaxis) of malaria caused by Plasmodium falciparum, including chloroquine-resistant strains.1 2 5 6 9 10 11 18 19 Recommended by CDC and others as a drug of choice for prophylaxis in individuals traveling to areas where chloroquine-resistant P. falciparum malaria has been reported;2 11 19 recommended by CDC as an alternative in those traveling to areas where chloroquine-resistant P. falciparum has not been reported.11


Treatment of acute, uncomplicated malaria caused by P. falciparum, including malaria acquired in areas where chloroquine resistance has been reported;1 2 7 8 13 14 18 21 has been effective in regions with multidrug-resistant P. falciparum malaria.1 18 Recommended by CDC as a drug of choice for treatment of uncomplicated chloroquine-resistant P. falciparum malaria.21


Presumptive self-treatment of malaria in travelers who elect not to use prophylaxis, those who require or choose to use a prophylaxis regimen that may not have optimal efficacy, or for long-term travelers receiving effective prophylaxis who plan to visit very remote areas.2 11 18 Recommended by CDC and others as drug of choice for such treatment.2 11


One of several regimens recommended by CDC for treatment of uncomplicated chloroquine-resistant P. vivax malaria.21


Active only against the asexual erythrocytic forms of Plasmodium (not exoerythrocytic stages) and cannot prevent delayed primary attacks or relapse of P. ovale or P. vivax malaria or provide a radical cure;3 4 11 primaquine usually also indicated to eradicate hypnozoites and prevent relapse in patients exposed to or being treated for P. ovale or P. vivax malaria.11


Detailed recommendations regarding prevention of malaria available from CDC 24 hours a day from the voice information service (877-394-8747) or at .11


Assistance with diagnosis or treatment of malaria available by contacting CDC Malaria Hotline at 770-488-7788 from 8:00 a.m. to 4:30 p.m. Eastern Standard Time or CDC Emergency Operation Center at 770-488-7100 after hours, on weekends, and holidays.21


Atovaquone and Proguanil Hydrochloride Dosage and Administration


Administration


Oral Administration


Administer orally with food or milky drink.1 2 18


Usually once daily as a single dose, given at the same time each day.1 18 When used for treatment of malaria, nausea and vomiting may be reduced by administering the daily dose in 2 equally divided doses.2


If vomiting occurs within 1 hour of ingestion, repeat dose.1 Antiemetic agents may be used if necessary.1 (See Drug Interactions: Metoclopramide.)


For children who have difficulty swallowing tablets, the tablets may be crushed and mixed with condensed milk just prior to administration.1 Tablets are not palatable if chewed due to bitter taste of proguanil.17


Dosage


Available as fixed combination containing atovaquone and proguanil hydrochloride; dosage expressed in terms of both drugs.1


Pediatric Patients


Prevention of Malaria

Oral

















Pediatric Dosage for Prevention of Malaria121118

Weight (kg)



Daily Dosage (Atovaquone/Proguanil HCL)



Dosage Regimen



11–20



62.5 mg/25 mg



1 pediatric tablet daily



21–30



125 mg/50 mg



2 pediatric tablets once daily



31–40



187.5 mg/75 mg



3 pediatric tablets once daily



>40



250 mg/100 mg



1 adult tablet daily


Initiate prophylaxis 1–2 days prior to entering the malarious area and continue for 7 days after leaving the area.1 2 11 18 19


Terminal prophylaxis with primaquine may also be indicated if exposure occurred in areas where P. ovale or P. vivax are endemic.2 11 Primaquine terminal prophylaxis generally is administered during the final 7 days of the atovaquone and proguanil regimen and then for an additional 7 days or, alternatively, for 14 days after the drug is discontinued.11


Treatment of Uncomplicated Malaria

Oral























Pediatric Dosage for Treatment of Acute, Uncomplicated Malaria121820

Weight (kg)



Daily Dosage (Atovaquone/Proguanil HCL)



Dosage Regimen



5–8



125 mg/50 mg



2 pediatric tablets daily for 3 consecutive days



9–10



187.5 mg/75 mg



3 pediatric tablets daily for 3 consecutive days



11–20



250 mg/100 mg



1 adult tablet daily for 3 consecutive days



21–30



500 mg/200 mg



2 adult tablets once daily for 3 consecutive days



31–40



750 mg/300 mg



3 adult tablets once daily for 3 consecutive days



>40



1 g/400 mg



4 adult tablets as a single daily dose for 3 consecutive days or 2 adult tablets twice daily for 3 consecutive days


Presumptive Self-treatment of Malaria

Oral

Use usual pediatric dosage recommended for treatment of uncomplicated malaria.2 11 18 Initiate presumptive self-treatment if malaria is suspected (fever, chills, or other influenza-like illness) and professional medical care will not be available within 24 hours.11 18


Not recommended for presumptive self-treatment of malaria in those currently taking the drug for prophylaxis.11


Adults


Prevention of Malaria

Oral

250 mg of atovaquone and 100 mg of proguanil hydrochloride (1 adult tablet) once daily.1 2 11 18 19


Initiate prophylaxis 1–2 days prior to entering the malarious area and continue for 7 days after leaving the area.1 2 11 18


Terminal prophylaxis with primaquine may also be indicated if exposure occurred in areas where P. ovale or P. vivax are endemic.2 11 Primaquine terminal prophylaxis generally is administered during the final 7 days of the atovaquone and proguanil regimen and then for an additional 7 days or, alternatively, for 14 days after the drug is discontinued.11


Treatment of Uncomplicated Malaria

Oral

1 g of atovaquone and 400 mg of proguanil hydrochloride (4 adult tablets) once daily for 3 consecutive days.1 2 20 Alternatively, 500 mg of atovaquone and 200 mg of proguanil hydrochloride (2 adult tablets) every 12 hours for 3 consecutive days.2


Presumptive Self-treatment of Malaria

Oral

Use usual adult dosage recommended for the treatment of malaria.2 11 18 Initiate presumptive self-treatment if malaria is suspected (fever, chills, or other influenza-like illness) and professional medical care will not be available within 24 hours.11 18


Not recommended for presumptive self-treatment of malaria in those currently taking the drug for prophylaxis.11


Special Populations


Renal Impairment


No dosage adjustments needed in those with mild to moderate renal impairment (Clcr 30–80 mL/minute).1


Geriatric Patients


Cautious dosage adjustment recommended.1


Cautions for Atovaquone and Proguanil Hydrochloride


Contraindications



  • Known hypersensitivity to atovaquone, proguanil, or any ingredient in the formulation.1




  • Prevention of malaria in patients with Clcr <30 mL/minute.1



Warnings/Precautions


Sensitivity Reactions


Anaphylaxis reported rarely.1 8 17


Erythema multiforme and Stevens-Johnson syndrome reported rarely.1 19 Rash and urticaria also reported.1


General Precautions


Hepatic Effects

Elevations in liver function test values reported.1 Hepatitis reported rarely.1 Hepatic failure requiring liver transplantation reported in at least one individual receiving the drug for prophylaxis.1


GI Effects

Atovaquone absorption reduced in patients with vomiting or diarrhea.1 Monitor for parasitemia and consider administration of an antiemetic agent.1 (See Drug Interactions: Metoclopramide.) Consider alternative antimalarial therapy if severe or persistent vomiting or diarrhea occurs.1


Severe Malaria

Not recommended for patients with cerebral malaria or other manifestations of severe complicated malaria (e.g., hyperparasitemia, pulmonary edema, renal failure).1


Prior Use

Repeated use not recommended following failure of the drug for treatment of malaria.1


Should not be used for treatment of malaria (including presumptive self-treatment) in patients who received the drug for prophylaxis of malaria.11 18


Other Precautions

Do not administer with other preparations containing proguanil.1


Specific Populations


Pregnancy

Category C.1


May be used in pregnant women if the potential benefits outweigh the possible risks to the fetus.1 18 CDC states that the drug may be used in pregnant women for treatment of uncomplicated malaria caused by chloroquine-resistant P. falciparum if other treatment options are not available or are not tolerated and if potential benefits outweigh risks.21 However, CDC states do not use for prevention of malaria in pregnant women.11


Lactation

Atovaquone distributed into milk in rats; proguanil distributed into human milk.1


Caution advised.1 May be used for treatment of malaria in women breast-feeding infants of any weight when the potential benefits outweigh the possible risks to the infant (e.g., when a breast-feeding woman has acquired P. falciparum malaria in an area with multidrug-resistant malaria and other treatment options are not tolerated).11 However, CDC states the drug should not be used for prevention of malaria in women breast-feeding infants who weigh <5 kg.11


Pediatric Use

Safety and efficacy for prevention of malaria not established in children weighing <11 kg.1


Safety and efficacy for treatment of malaria not established in children weighing <5 kg.1 20


Geriatric Use

Insufficient experience in patients ≥65 years of age to determine whether geriatric patients respond differently than younger adults; select dosage with caution.1


Hepatic Impairment

Use with caution in severe hepatic impairment.17


Renal Impairment

Contraindicated for prevention of malaria if Clcr <30 mL/minute.


Use with caution for treatment of malaria if Clcr <30 mL/minute and only if benefits outweigh risks (e.g., increased drug concentrations).1


Common Adverse Effects


Abdominal pain, nausea, vomiting, headache, diarrhea, asthenia, anorexia, dizziness, cough, and pruritus.1


Interactions for Atovaquone and Proguanil Hydrochloride


Proguanil metabolized principally by CYP2C19; potential pharmacokinetic interactions with other substrates or inhibitors of this enzyme unknown.1


Protein-Bound Drugs


Pharmacokinetic interaction unlikely.1


Specific Drugs





















Drug



Interaction



Comments



Antimycobacterials, rifamycins (rifabutin, rifampin)



Decreased plasma atovaquone concentrations1



Concomitant use not recommended1



Indinavir



Decreased trough concentrations of indinavir; no change in peak plasma concentrations or AUC of indinavir1



Use with caution1



Metoclopramide



Decreased bioavailability of atovaquone1



Use concomitantly only if other antiemetics not available1



Tetracycline



Decreased plasma atovaquone concentrations1



Closely monitor parasitemia1



Warfarin



Possible potentiation of the anticoagulant effects of warfarin1



Monitor coagulation parameters1


Atovaquone and Proguanil Hydrochloride Pharmacokinetics


Absorption


Bioavailability


Oral bioavailability of atovaquone shows considerable interindividual variation;1 absorption of atovaquone may be reduced in patients with diarrhea and vomiting.1 Proguanil hydrochloride extensively absorbed from the GI tract.1


Food


Administration with dietary fat increases the rate and extent of GI absorption of atovaquone;1 absolute bioavailability is 23% when taken with food.1


GI absorption of proguanil hydrochloride not affected by food.1


Distribution


Extent


Atovaquone distributed into milk in rats; not known whether the drug distributed into human milk.1 Small amounts of proguanil are distributed into milk.1


Plasma Protein Binding


Atovaquone is >99% bound to plasma proteins; proguanil is 75% bound to plasma proteins.1


Elimination


Metabolism


There is indirect evidence that atovaquone may undergo limited metabolism; however, a specific metabolite(s) has not been identified.1 Proguanil metabolized principally by CYP2C19 to the active metabolite cycloguanil and to 4-chlorophenylbiguanide.1


Elimination Route


Following oral administration in healthy individuals, >94% of a dose of atovaquone excreted unchanged in feces; 40–60% of a dose of proguanil excreted in urine.1


Half-life


Atovaquone: Elimination half-life is about 2–3 days in adults and 1–2 days in pediatric patients.1


Proguanil: Elimination half-life is 12–21 hours in adult and pediatric patients;1 may be longer in slow metabolizers.1


Special Populations


In patients with mild to moderate hepatic impairment, there were no marked differences in the rate or extent of systemic exposure to atovaquone, although the elimination half-life of atovaquone was prolonged in individuals with moderate hepatic impairment.1 In patients with mild to moderate hepatic impairment, the extent of systemic exposure to proguanil was increased and the elimination half-life was prolonged, with a resultant decrease in systemic exposure to cycloguanil and an increase in the elimination half-life of this metabolite.1


Pharmacokinetics of atovaquone and proguanil in patients with mild renal impairment (Clcr 50–80 mL/minute) similar to that in those with normal renal function.1 In patients with moderate renal impairment (Clcr 30–50 mL/minute), oral clearance of atovaquone unaffected but proguanil oral clearance reduced approximately 35%.1


In patients with severe renal impairment (Clcr <30 mL/minute), systemic exposure to atovaquone was decreased and elimination half-lives of proguanil and cycloguanil were increased, resulting in the potential for drug accumulation and toxicity with repeated dosing.1


In geriatric individuals (65–79 years of age), the extent of systemic exposure to cycloguanil (active metabolite of proguanil) was increased, and the average elimination half-life was prolonged (mean: 14.9 hours) compared with younger adults (mean: 8.3 hours).1


Stability


Storage


Oral


Tablets

25°C (may be exposed to 15–30°C).1


Actions and SpectrumActions



  • A fixed combination of 2 antimalarial agents: atovaquone (a hydroxynaphthoquinone derivative)4 5 and proguanil hydrochloride (a biguanide derivative).1 2 3 4 5 6 7 8 9 10 13 14 15




  • Atovaquone selectively inhibits mitochondrial electron transport in plasmodia and collapses mitochondrial membrane potential.1 5 6 7 8 10 Antimalarial activity of proguanil principally due to its active metabolite (cycloguanil);1 4 6 7 cycloguanil inhibits dihydrofolate reductase, leading to depletion of pyrimidine nucleotide pools and disruption in nucleic acid synthesis and cell replication.1 4 6 10




  • Atovaquone and proguanil synergistic against erythrocytic stages of Plasmodium.5 6 7 13 Proguanil may lower concentration of atovaquone needed to collapse mitochondrial membrane potential.15




  • Active against erythrocytic forms of most strains of Plasmodium falciparum, P. malariae, P. ovale, and P. vivax1 8 and exoerythrocytic forms of Plasmodium;1 no activity against P. vivax hypnozoites.3 8




  • P. falciparum with decreased susceptibility to atovaquone or to proguanil/cycloguanil can be selected in vitro or in vivo.1



Advice to Patients



  • Importance of taking atovaquone and proguanil at the same time each day with food or milky drink.1




  • Importance of repeating dose if vomiting occurs within 1 hour of ingestion.1




  • Importance of consulting clinician regarding alternative prophylaxis regimens if atovaquone and proguanil prophylaxis is discontinued for any reason.1




  • Necessity of taking protective measures to reduce contact with mosquitoes (protective clothing, insect repellents, mosquito nets, remaining in air-conditioned or well-screened areas).1 11




  • Possibility of contracting malaria during travel, regardless of prophylactic regimen used.1 11




  • Advise travelers who plan presumptive self-treatment in the event of a possible malarial infection to keep an amount of atovaquone and proguanil sufficient for self-treatment in their possession during travel and to take it promptly in the event of a febrile illness during or after their travel if professional medical care is not readily available.2




  • Advise travelers that presumptive self-treatment of malaria is an interim measure and that they should seek medical evaluation as soon as possible.11 18




  • Importance of seeking medical attention as soon as possible if febrile illness develops during or after return from a malaria-endemic area and of informing clinician of possible malaria exposure, including instances when such illness was self-treated as malaria during travel.1 11




  • Advise patients of risk of rare serious adverse effects including hepatitis, severe skin reactions, neurologic events, or hematologic events.1




  • Importance of notifying clinician of existing or contemplated therapy, including prescription and OTC drugs1 and herbal or dietary supplements, and any concomitant illnesses.




  • Importance of women informing clinician if they are or plan to become pregnant or plan to breast-feed.1




  • Importance of discussing with clinician the risks and benefits of travel to malaria-endemic areas during pregnancy.1 Compared with other populations, pregnant women have higher risk of death and serious complications of falciparum malaria.1




  • Importance of advising patients of other important precautionary information.1 (See Cautions.)



Preparations


Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.


















Atovaquone and Proguanil Hydrochloride

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Oral



Tablets, film-coated



62.5 mg of atovaquone and 25 mg of proguanil hydrochloride



Malarone Pediatric



GlaxoSmithKline



250 mg of atovaquone and 100 mg of proguanil hydrochloride



Malarone



GlaxoSmithKline



Disclaimer

This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.


The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions January 2010. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.


† Use is not currently included in the labeling approved by the US Food and Drug Administration.




References



1. GlaxoSmithKline. Malarone (atovaquone and proguanil hydrochloride) tablets and pediatric tablets prescribing information. Research Triangle Park, NC; 2008 Jun.



2. Anon. Drugs for parasitic infections. From the Medical Letter website (). Aug 2008.



3. Anon. Atovaquone and proguanil hydrochloride: a new antimalarial combination. WHO Drug Information. 1999; 13:226-227.



4. Parfitt K, ed. Martindale: the complete drug reference. 32nd ed. London: The Pharmaceutical Press; 1999:422-42.



5. Shanks GD, Gordon DM, Klotz FW et al. Efficacy and safety of atovaquone/proguanil as suppressive prophylaxis for Plasmodium falciparum malaria. Clin Infect Dis. 1998; 27:494-9. [IDIS 419667] [PubMed 9770146]



6. Sukwa TY, Mulenga M, Chisdaka N et al. A randomized, double-blind, placebo-controlled field trial to determine the efficacy and safety of Malarone (atovaquone/proguanil) for the prophylaxis of malaria in Zambia. Am J Trop Med Hyg. 1999; 60:521-25. [IDIS 428139] [PubMed 10348223]



7. Bustos DG, Canfield CJ, Canete-Miquel E et al. Atovaquone-proguanil compared with chloroquine and chloroquine-sulfadoxine-pyrimethamine for treatment of acute Plasmodium falciparum malaria in the Philippines. J Infect Dis. 1999; 179:1587-90. [IDIS 430232] [PubMed 10228090]



8. Looareesuwan S, Chulay JD, Canfield CJ et al. Malarone (atovaquone and proguanil hydrochloride): a review of its clinical development for treatment of malaria. Am J Trop Med Hyg. 1999; 60:533-43. [IDIS 428141] [PubMed 10348225]



9. Lell B, Luckner D, Ndjaveé M et al. Randomised placebo-controlled study of atovaquone plus proguanil for malaria prophylaxis in children. Lancet. 1998; 351:709-13. [IDIS 402024] [PubMed 9504515]



10. van der Berg JD, Duvenage CSJ, Roskell NS et al. Safety and efficacy of atovaquone and proguanil hydrochloride for the prophylaxis of Plasmodium falciparum malaria in South Africa. Clin Ther. 1999; 21:741-9. [IDIS 428169] [PubMed 10363739]



11. Centers for Disease Control and Prevention. Health information for international travel, 2010. Atlanta, GA: US Department of Health and Human Services; 2010. Updates available from CDC website ().



12. WHO. International travel and health: vaccination requirements and health advice- situation as of Jan 1, 2000. Geneva: WHO; 2000:67-85.



13. Looareesuwan S, Wilairatana P, Chalermarut K et al. Efficacy and safety of atovaquone/proguanil compared with mefloquine for treatment of acute Plasmodium falciparum malaria in Thailand. Am J Trop Med Hyg. 1999; 60:526-32. [IDIS 428140] [PubMed 10348224]



14. Anabwani G, Canfield CJ, Hitchinson DBA. Combination atovaquone and proguanil hydrochloride vs halofantrine for treatment of acute Plasmodium falciparum malaria in children. Ped Infect Dis. 1999; 18:456-61.



15. Srivastava IK, Vaidya AB. A mechanism for the synergistic antimalarial action of atovaquone and proguanil. Antimicrob Agents Chemother. 1999; 43:1334-9. [PubMed 10348748]



17. Glaxo Wellcome, Research Triangle Park, NC: Personal communication.



18. Centers for Disease Control and Prevention. Information for health care providers: Malarone for malaria treatment and prophylaxis. From CDC web site (). Accessed Sept 25, 2003.



19. Anon. Advice for travelers. Med Lett Treat Guid. 2006; 45:25-34.



20. Centers for Disease Control and Prevention. CDC treatment guidelines: Treatment of malaria (guidelines for clinicians). 2007 Mar. From the CDC website: ().



21. Centers for Disease Control and Prevention. Guidelines for treatment of malaria in the United States (based on drugs currently available for use in the United States). From the CDC website: (). Accessed 2009 Jul 1.



More Atovaquone and Proguanil Hydrochloride resources


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  • Atovaquone and Proguanil Hydrochloride Dosage
  • Atovaquone and Proguanil Hydrochloride Use in Pregnancy & Breastfeeding
  • Atovaquone and Proguanil Hydrochloride Drug Interactions
  • Atovaquone and Proguanil Hydrochloride Support Group
  • 6 Reviews for Atovaquone and Proguanil Hydrochloride - Add your own review/rating


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  • Malaria
  • Malaria Prevention

Thursday, September 29, 2016

Penlac Solution


Pronunciation: sye-kloe-PEER-ox
Generic Name: Ciclopirox
Brand Name: Penlac


Penlac Solution is used for:

Treating mild to moderate toenail or fingernail fungus.


Penlac Solution is an antifungal agent. It is believed to work by slowing the growth of fungi.


Do NOT use Penlac Solution if:


  • you are allergic to any ingredient in Penlac Solution

  • you are taking an oral antifungal medicine, for a fungal infection of the fingernail or toenail

Contact your doctor or health care provider right away if any of these apply to you.



Before using Penlac Solution:


Some medical conditions may interact with Penlac Solution. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

  • if you have diabetes

Some MEDICINES MAY INTERACT with Penlac Solution. However, no specific interactions with Penlac Solution are known at this time.


Ask your health care provider if Penlac Solution may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Penlac Solution:


Use Penlac Solution as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Apply this medication evenly over the entire nail plate once daily and a small amount of the surrounding skin, preferably at bedtime or 8 hours before washing. If possible, apply this medication to the nail bed and under the surface of the nail plate.

  • Do not remove this medication on a daily basis. Daily applications of this medication should be made over the previous coat and removed every 7 days with alcohol.

  • Using an emery board, file away any loose nail material, and trim nails every 7 days after this medication is removed with alcohol.

  • This medication may need to be taken for up to 48 weeks in combination with nail removal done by your health care provider to achieve a clear or almost clear nail. It may take up to 6 months to see any noticeable improvement in your nail. However, a completely clear nail may not be achieved with the use of this medication.

  • To clear up your infection completely, use Penlac Solution for the full course of treatment.

  • If you miss a dose of Penlac Solution and you are using it daily at bedtime, skip the missed dose. Do not use the medicine the following morning. If you do not use the dose at bedtime and you miss a dose, use it as soon as possible. If several hours have passed or it is nearing time for the next dose, skip the missed dose and return to your regular dosing schedule.

Ask your health care provider any questions you may have about how to use Penlac Solution.



Important safety information:


  • For use on nails and surrounding skin only. Do not get Penlac Solution in your eyes, nose, or mouth. If you get it in your eyes, rinse right away with cool tap water.

  • Penlac Solution may cause harm if it is swallowed. If you may have taken it by mouth, contact your poison control center or emergency room right away.

  • Do not use nail polish or other nail cosmetic products while using this medication.

  • Do not use this medication near heat or open flame because this medication is flammable.

  • PREGNANCY AND BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Penlac Solution while you are pregnant. It is not known if Penlac Solution is found in breast. If you are or will be breast-feeding while you use Penlac Solution, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Penlac Solution:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Change in shape of nail; discoloration; ingrown toenail; irritation; redness of the treated area.



Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blistering; burning; increased redness; itching; oozing of the treated area; rash on the palms; swelling.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Penlac side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Penlac Solution may be harmful if swallowed.


Proper storage of Penlac Solution:

Store Penlac Solution at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Protect from light. Keep away from heat and flame. Keep Penlac Solution out of the reach of children and away from pets.


General information:


  • If you have any questions about Penlac Solution, please talk with your doctor, pharmacist, or other health care provider.

  • Penlac Solution is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

  • Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Penlac Solution. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Penlac resources


  • Penlac Side Effects (in more detail)
  • Penlac Use in Pregnancy & Breastfeeding
  • Penlac Support Group
  • 1 Review for Penlac - Add your own review/rating


Compare Penlac with other medications


  • Onychomycosis, Fingernail
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Proventil HFA



albuterol sulfate

Dosage Form: inhalation aerosol
PROVENTIL® HFA

(albuterol sulfate)

Inhalation Aerosol

FOR ORAL INHALATION ONLY


Prescribing Information



DESCRIPTION


The active component of PROVENTIL® HFA (albuterol sulfate) Inhalation Aerosol is albuterol sulfate, USP racemic α1 [(tert-Butylamino)methyl]-4-hydroxy-m-xylene-α,α'-diol sulfate (2:1)(salt), a relatively selective beta2-adrenergic bronchodilator having the following chemical structure:



Albuterol sulfate is the official generic name in the United States. The World Health Organization recommended name for the drug is salbutamol sulfate. The molecular weight of albuterol sulfate is 576.7, and the empirical formula is (C13H21 NO3)2•H2SO4. Albuterol sulfate is a white to off-white crystalline solid. It is soluble in water and slightly soluble in ethanol. Proventil HFA Inhalation Aerosol is a pressurized metered-dose aerosol unit for oral inhalation. It contains a microcrystalline suspension of albuterol sulfate in propellant HFA-134a (1,1,1,2-tetrafluoroethane), ethanol, and oleic acid.


Each actuation delivers 120 mcg albuterol sulfate, USP from the valve and 108 mcg albuterol sulfate, USP from the mouthpiece (equivalent to 90 mcg of albuterol base from the mouthpiece). Each canister provides 200 inhalations. It is recommended to prime the inhaler before using for the first time and in cases where the inhaler has not been used for more than 2 weeks by releasing four “test sprays” into the air, away from the face.


This product does not contain chlorofluorocarbons (CFCs) as the propellant.



CLINICAL PHARMACOLOGY



Mechanism of Action  In vitro studies and in vivo pharmacologic studies have demonstrated that albuterol has a preferential effect on beta2-adrenergic receptors compared with isoproterenol. While it is recognized that beta2-adrenergic receptors are the predominant receptors on bronchial smooth muscle, data indicate that there is a population of beta2-receptors in the human heart existing in a concentration between 10% and 50% of cardiac beta-adrenergic receptors. The precise function of these receptors has not been established. (See WARNINGS, Cardiovascular Effects section.)


Activation of beta2-adrenergic receptors on airway smooth muscle leads to the activation of adenylcyclase and to an increase in the intra-cellular concentration of cyclic-3',5'-adenosine monophosphate (cyclic AMP). This increase of cyclic AMP leads to the activation of protein kinase A, which inhabits the phosphorylation of myosin and lowers intracellular ionic calcium concentrations, resulting in relaxation. Albuterol relaxes the smooth muscles of all airways, from the trachea to the terminal bronchioles. Albuterol acts as a functional antagonist to relax the airway irrespective of the spasmogen involved, thus protecting against all bronchoconstricor challenges. Increased cyclic AMP concentrations are also associated with the inhibition of release of mediators from mast cells in the airway.


Albuterol has been shown in most clinical trials to have more effect on the respiratory tract, in the form of bronchial smooth muscle relaxation, than isoproterenol at comparable doses while producing fewer cardiovascular effects. Controlled clinical studies and other clinical experience have shown that inhaled albuterol, like other beta-adrenergic agonist drugs, can produce a significant cardiovascular effect in some patients, as measured by pulse rate, blood pressure, symptoms, and/or electrocardiographic changes.



Preclinical  Intravenous studies in rats with albuterol sulfate have demonstrated that albuterol crosses the blood-brain barrier and reaches brain concentrations amounting to approximately 5% of the plasma concentrations. In structures outside the blood-brain barrier (pineal and pituitary glands), albuterol concentrations were found to be 100 times those in the whole brain.


Studies in laboratory animals (minipigs, rodents, and dogs) have demonstrated the occurrence of cardiac arrhythmias and sudden death (with histologic evidence of myocardial necrosis) when beta2-agonist and methylxanthines were administered concurrently. The clinical significance of these findings is unknown.


Propellant HFA-134a is devoid of pharmacological activity except at very high doses in animals (380-1300 times the maximum human exposure based on comparisons of AUC values), primarily producing ataxia, tremors, dyspnea, or salivation. These are similar to effects produced by the structurally related chlorofluorocarbons (CFCs), which have been used extensively in metered dose inhalers.


In animals and humans, propellant HFA-134a was found to be rapidly absorbed and rapidly eliminated, with an elimination half-life of 3 to 27 minutes in animals and 5 to 7 minutes in humans. Time to maximum plasma concentration (Tmax) and mean residence time are both extremely short, leading to a transient appearance of HFA-134a in the blood with no evidence of accumulation.



Pharmacokinetics  In a single-dose bioavailability study which enrolled six healthy, male volunteers, transient low albuterol levels (close to the lower limit of quantitation) were observed after administration of two puffs from both PROVENTIL® HFA Inhalation Aerosol and a CFC 11/12 propelled albuterol inhaler. No formal pharmacokinetic analyses were possible for either treatment, but systemic albuterol levels appeared similar.



Clinical Trials  In a 12-week, randomized, double-blind, double-dummy, active- and placebo-controlled trial, 565 patients with asthma were evaluated for the bronchodilator efficacy of Proventil HFA Inhalation Aerosol (193 patients) in comparison to a CFC 11/12 propelled albuterol inhaler (186 patients) and an HFA-134a placebo inhaler (186 patients).


Serial FEV1 measurements (shown below as percent change from test-day baseline) demonstrated that two inhalations of Proventil HFA Inhalation Aerosol produced significantly greater improvement in pulmonary function than placebo and produced outcomes which were clinically comparable to a CFC 11/12 propelled albuterol inhaler.


The mean time to onset of a 15% increase in FEV1 was 6 minutes and the mean time to peak effect was 50 to 55 minutes. The mean duration of effect as measured by a 15% increase in FEV1 was 3 hours. In some patients, duration of effect was as long as 6 hours.


In another clinical study in adults, two inhalations of Proventil HFA Inhalation Aerosol taken 30 minutes before exercise prevented exercise-induced bronchospasm as demonstrated by the maintenance of FEV1 within 80% of baseline values in the majority of patients.


In a 4-week, randomized, open-label trial, 63 children, 4 to 11 years of age, with asthma were evaluated for the bronchodilator efficacy of Proventil HFA Inhalation Aerosol (33 pediatric patients) in comparison to a CFC 11/12 propelled albuterol inhaler (30 pediatric patients).



Serial FEV1 measurements as percent change from test-day baseline demonstrated that two inhalations of Proventil HFA Inhalation Aerosol produced outcomes which were clinically comparable to a CFC 11/12 propelled albuterol inhaler.


The mean time to onset of a 12% increase in FEV1 for Proventil HFA Inhalation Aerosol was 7 minutes and the mean time to peak effect was approximately 50 minutes. The mean duration of effect as measured by a 12% increase in FEV1 was 2.3 hours. In some pediatric patients, duration of effect was as long as 6 hours.


In another clinical study in pediatric patients, two inhalations of Proventil HFA Inhalation Aerosol taken 30 minutes before exercise provided comparable protection against exercise-induced bronchospasm as a CFC 11/12 propelled albuterol inhaler.



INDICATIONS AND USAGE


PROVENTIL® HFA Inhalation Aerosol is indicated in adults and children 4 years of age and older for the treatment or prevention of bronchospasm with reversible obstructive airway disease and for the prevention of exercise-induced bronchospasm.



CONTRAINDICTIONS


PROVENTIL® HFA Inhalation Aerosol is contraindicated in patients with a history of hypersensitivity to albuterol or any other Proventil HFA components.



WARNINGS


  1. Paradoxical Bronchospasm: Inhaled albuterol sulfate can produce paradoxical bronchospasm that may be life threatening. If paradoxical bronchospasm occur, PROVENTIL® HFA Inhalation Aerosol should be discontinued immediately and alternative therapy instituted. It should be recognized that paradoxical bronchospasm, when associated with inhaled formulations, frequently occurs with the first use of a new canister.

  2. Deterioration of Asthma: Asthma may deteriorate acutely over a period of hours or chronically over several days or longer. If the patient needs more doses of Proventil HFA Inhalation Aerosol than usual, this may be a marker of destabilization of asthma and requires re-evaluation of the patient and treatment regimen, giving special consideration to the possible need for anti-inflammatory treatment, eg, corticosteroids.

  3. Use of Anti-inflammatory Agents: The use of beta-adrenergic-agonist bronchodilators alone may not be adequate to control asthma in many patients. Early consideration should be given to adding anti-inflammatory agents, eg, corticosteroids, to the therapeutic regimen.

  4. Cardiovascular Effects: Proventil HFA Inhalation Aerosol, like other beta-adrenergic agonist, can produce clinically significant cardiovascular effects in some patients as measured by pulse rate, blood pressure, and/or symptoms. Although such effects are uncommon after administration of Proventil HFA Inhalation Aerosol at recommended doses, if they occur, the drug may need to be discontinued. In addition, beta-agonists have been reported to produce ECG changes, such as flattening of the T wave, prolongation of the QTc interval, and ST segment depression. The clinical significance of these findings is unknown. Therefore, Proventil HFA Inhalation Aerosol, like all sympathomimetic amines, should be used with caution in patients with cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, and hypertension.

  5. Do Not Exceed Recommended Dose: Fatalities have been reported in association with excessive use of inhaled sympathomimetic drugs in patients with asthma. The exact cause of death is unknown, but cardiac arrest following an unexpected development of a severe acute asthmatic crisis and subsequent hypoxia is suspected.

  6. Immediate Hypersensitivity Reactions: Immediate hypersensitivity reactions may occur after administration of albuterol sulfate, as demonstrated by rare cases of urticaria, angioedema, rash, bronchospasm, anaphylaxis, and oropharyngeal edema.


PRECAUTIONS



General Albuterol sulfate, as with all sympathomimetic amines, should be used with caution in patients with cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, and hypertension; in patients with convulsive disorders, hyperthyroidism, or diabetes mellitus; and in patients who are unusually responsive to sympathomimetic amines. Clinically significant changes in systolic and diastolic blood pressure have been seen in individual patients and could be expected to occur in some patients after use of any beta-adrenergic bronchodilator.


Large doses of intravenous albuterol have been reported to aggravate preexisting diabetes mellitus and ketoacidosis. As with other beta-agonists, albuterol may produce significant hypokalemia in some patients, possibly through intracellular shunting, which has the potential to produce adverse cardiovascular effects. The decrease is usually transient, not requiring supplementation.



Information for Patients See illustrated Patient's Instructions for Use. SHAKE WELL BEFORE USING. Patients should be given the following information:


It is recommended to prime the inhaler before using for the first time and in cases where the inhaler has not been used for more than 2 weeks by releasing four “test sprays” into the air, away from the face.


KEEPING THE PLASTIC MOUTHPIECE CLEAN IS VERY IMPORTANT TO PREVENT MEDICATION BUILD-UP AND BLOCKAGE. THE MOUTHPIECE SHOULD BE WASHED, SHAKEN TO REMOVE EXCESS WATER, AND AIR DRIED THOROUGHLY AT LEASE ONCE A WEEK. INHALER MAY CEASE TO DELIVER MEDICATION IF NOT PROPERLY CLEANED.


The mouthpiece should be cleaned (with the canister removed) by running warm water through the top and bottom for 30 seconds at least once a week. The mouthpiece must be shaken to remove excess water, then air dried thoroughly (such as overnight). Blockage from medication build-up or improper medication delivery may result from failure to thoroughly air dry the mouthpiece.


If the mouthpiece should become blocked (little or no medication coming out of the mouthpiece), the blockage may be removed by washing as described above.


If it is necessary to use the inhaler before it is completely dry, shake off excess water, replace canister, test spray twice away from face, and take the prescribed dose. After such use, the mouthpiece should be rewashed and allowed to air dry thoroughly.


The action of PROVENTIL® HFA Inhalation Aerosol should last up to 4 to 6 hours. Proventil HFA Inhalation Aerosol should not be used more frequently than recommended. Do not increase the dose or frequency of doses of Proventil HFA Inhalation Aerosol without consulting your physician. If you find that treatment with Proventil HFA Inhalation Aerosol becomes less effective for symptomatic relief, your symptoms become worse, and/or you need to use the product more frequently than usual, medical attention should be sought immediately. While you are taking Proventil HFA Inhalation Aerosol, other inhaled drugs and asthma medications should be taken only as directed by your physician.


Common adverse effects of treatment with inhaled albuterol include palpitations, chest pain, rapid heart rate, tremor, or nervousness. If you are pregnant or nursing, contact your physician about use of Proventil HFA Inhalation Aerosol. Effective and safe use of Proventil HFA Inhalation Aerosol includes an understanding of the way that it should be administered. Use Proventil HFA Inhalation Aerosol only with the actuator supplied with the product. Discard the canister after 200 sprays have been used.


In general, the technique for administering Proventil HFA Inhalation Aerosol to children is similar to that for adults. Children should use Proventil HFA Inhalation Aerosol under adult supervision, as instructed by the patient's physician. (See Patient's Instructions for Use).



Drug Interactions


  1. Beta-Blockers: Beta-adrenergic-receptor blocking agents not only block the pulmonary effect of beta-agonists, such as Proventil HFA Inhalation Aerosol, but may produce severe bronchospasm in asthmatic patients. Therefore, patients with asthma should not normally be treated with beta-blockers. However, under certain circumstances, eg, as prophylaxis after myocardial infarction, there may be no acceptable alternatives to the use of beta-adrenergic blocking agents in patients with asthma. In this setting, cardioselective beta blockers should be considered, although they should be administered with caution.

  2. Diuretics: The ECG changes and/or hypokalemia which may result from the administration of nonpotassium-sparing diuretics (such as loop or thiazide diuretics) can be acutely worsened by beta-agonists, especially when the recommended dose of the beta-agonist is exceeded. Although the clinical significance of these effects is not known, caution is advised in the coadministration of beta agonists with nonpotassium-sparing diuretics.

  3. Albuterol-Digoxin: Mean decreases of 16% and 22% in serum digoxin levels were demonstrated after single-dose intravenous and oral administration of albuterol, respectively, to normal volunteers who had received digoxin for 10 days. The clinical significance of these findings for patients with obstructive airway disease who are receiving albuterol and digoxin on a chronic basis is unclear; nevertheless, it would be prudent to carefully evaluate the serum digoxin levels in patients who are currently receiving digoxin and albuterol.

  4. Monoamine Oxidase Inhibitors or Tricyclic Antidepressants: Proventil HFA Inhalation Aerosol should be administered with extreme caution to patients being treated with monoamine oxidase inhibitors or tricyclic antidepressants, or within 2 weeks of discontinuation of such agents, because the action of albuterol on the cardiovascular system may be potentiated.


Carcinogenesis, Mutagenesis, and Impairment of Fertility


In a 2-year study in SPRAGUE-DAWLEY® rats, albuterol sulfate caused a dose-related increase in the incidence of benign leiomyomas of the mesovarium at the above dietary doses of 2 mg/kg (approximately 15 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 6 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). In another study this effect was blocked by the coadministration of propranolol, a nonselective beta-adrenergic antagonist. In an 18-month study in CD-1 mice, albuterol sulfate showed no evidence of tumorigenicity at dietary doses of up to 500 mg/kg (approximately 1700 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 800 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). In a 22-month study in Golden Hamsters, albuterol sulfate showed no evidence of tumorigenicity at dietary doses of up to 50 mg/kg (approximately 225 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 110 times the maximum recommended daily inhalation dose for children on a mg/m2 basis).


Albuterol sulfate was not mutagenic in the Ames test or a mutation test in yeast. Albuterol sulfate was not clastogenic in a human peripheral lymphocyte assay or in an AH1 strain mouse micronucleus assay.


Reproduction studies in rats demonstrated no evidence of impaired fertility at oral doses up to 50 mg/kg (approximately 340 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis).



Pregnancy: Teratogenic Effects: Pregnancy Category C


Albuterol sulfate has been shown to be teratogenic in mice. A study in CD-1 mice given albuterol sulfate subcutaneously showed cleft palate formation in 5 of 111 (4.5%) fetuses at 0.25 mg/kg (less than the maximum recommended daily inhalation dose for adults on a mg/m2 basis) and in 10 of 108 (9.3%) fetuses at 2.5 mg/kg (approximately 8 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis). The drug did not induce cleft palate formation at a dose of 0.025 mg/kg (less than the maximum recommended daily inhalation dose for adults on a mg/m2 basis). Cleft palate also occurred in 22 of 72 (30.5%) fetuses from females treated subcutaneously with 2.5 mg/kg of isoproterenol (positive control).


A reproduction study in Stride Dutch rabbits revealed cranioschisis in 7 of 19 (37%) fetuses when albuterol sulfate was administered orally at 50 mg/kg dose (approximately 680 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis).


In an inhalation reproduction study in SPRAGUE-DAWLEY rats, the albuterol sulfate/HFA-134a formulation did not exhibit any teratogenic effects at 10.5 mg/kg (approximately 70 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis).


A study in which pregnant rats were dosed with radiolabeled albuterol sulfate demonstrated that drug-related material is transferred from the maternal circulation to the fetus.


There are no adequate and well-controlled studies of Proventil HFA Inhalation Aerosol or albuterol sulfate in pregnant women. Proventil HFA Inhalation Aerosol should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.


During worldwide marketing experience, various congenital anomalies, including cleft palate and limb defects, have been reported in the offspring of patients being treated with albuterol. Some of the mothers were taking multiple medications during their pregnancies. Because no consistent pattern of defects can be discerned, a relationship between albuterol use and congenital anomalies has not been established.



Use in Labor and Delivery


Because of the potential for beta-agonist interference with uterine contractility, use of Proventil HFA Inhalation Aerosol for relief of bronchospesm during labor should be restricted to those patients in whom the benefits clearly outweigh the risk.



Tocolysis: Albuterol has not been approved for the management of preterm labor. The benefit:risk ratio when albuterol is administered for tocolysis has not been established. Serious adverse reactions, including pulmonary edema, have been reported during the following treatment of premature labor with beta2-agonists, including albuterol.



Nursing Mothers


Plasma levels of albuterol sulfate and HFA-134a after inhaled therapeutic doses are very low in humans, but it is not known whether the components of Proventil HFA Inhalation Aerosol are excreated in human milk.


Because of the potential for tumorigenicity shown for albuterol in animal studies and lack of experience with the use of Proventil HFA Inhalation Aerosol by nursing mothers, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother. Caution should be exercised when albuterol sulfate is administered to a nursing woman.



Pediatrics


The safety and effectiveness of Proventil HFA Inhalation Aerosol in pediatric patients below the age of 4 years have not been established.



Geriatrics


Proventil HFA Inhalation Aerosol has not been studied in a geriatric population. As with other beta2-agonists, special caution should be observed when using Proventil HFA Inhalation Aerosol in elderly patients who have concomitant cardiovascular disease that could be adversely affected by this class of drug.



Adverse Reactions


Adverse reaction information concerning PROVENTIL® HFA Inhalation Aerosol is derived from a 12-week, double-blind, double-dummy study which compared Proventil HFA Inhalation Aerosol, a CFC 11/12 propelled albuterol inhaler, and an HFA-134a placebo inhaler in 565 asthmatic patients. The following table lists the incidence of all adverse events (whether considered by the investigator drug related or unrelated to drug) from this study which occurred at a rate of 3% or greater in the Proventil HFA Inhalation Aerosol treatment group and more frequently in the Proventil HFA Inhalation Aerosol treatment group than in the placebo group. Overall, the incidence and nature of the adverse reactions reported for Proventil HFA Inhalation Aerosol and a CFC 11/12 propelled albuterol inhaler were comparable.




















































































Adverse Experience Incidences (% of patients) in a Large 12-week Clinical Trial*
Body System/

Adverse Event (Preferred Term)
PROVENTIL® HFA Inhalation Aerosol (N=193)CFC 11/12 Propelled Albuterol Inhaler (N=186)HFA-134a Placebo Inhaler (N=186)

*This table includes all adverse events (whether considered by the investigator drug related or unrelated to drug) which occurred at an incidence rate of at least 3.0% in the Proventil HFA Inhalation Aerosol group and more frequently in the Proventil HFA Inhalation Aerosol group than in the HFA-134a placebo inhaler group.


Application Site DisordersInhalation Site Sensation692
Inhalation Taste Sensation433
Body as a WholeAllergic Reaction/Symptoms64<1
Back Pain423
Fever625
Central and Peripheral Nervous SystemTremor782
Gastrointestinal SystemNausea1095
Vomiting723
Heart Rate and Rhythm DisorderTachycardia72<1
Psychiatric DisordersNervousness793
Respiratory System DisordersRespiratory Disorder
(unspecified)645
Rhinitis162214
Upper Resp Tract Infection212018
Urinary System DisorderUrinary Tract Infection342

Adverse events reported by less than 3% of the patients receiving Proventil HFA Inhalation Aerosol, and by a greater proportion of Proventil HFA Inhalation Aerosol patients than placebo patients, which have the potential to be related to Proventil HFA Inhalation Aerosol include: dysphonia, increased sweating, dry mouth, chest pain, edema, rigors, ataxia, leg cramps, hyperkinesia, eructation, flatulence, tinnitus, diabetes mellitus, anxiety, depression, somnolence, rash. Palpitation and dizziness have also been observed with Proventil HFA Inhalation Aerosol.


Adverse events reported in a 4-week pediatric clinical trail comparing Proventil HFA Inhalation Aerosol and a CFC 11/12 propelled albuterol inhaler occurred at a low incidence rate and were similar to those seen in the adult trials.


In small, cumulative dose studies, tremor, nervousness, and headache appeared to be dose related.


Rare cases of urticaria, angioedema, rash, bronchospasm, and oropharyngeal edema have been reported after the use of inhaled albuterol. In addition, albuterol, like other sympathomimetic agents, can cause adverse reactions such as hypertension, angina, vertigo, central nervous system stimulation, insomnia, headache, and drying or irritation of the oropharynx.



OVERDOSE


The expected symptoms with overdosage are those of excessive beta-adrenergic stimulation and/or occurrence or exaggeration of any of the symptoms listed under ADVERSE REACTIONS, eg, seizures, angina, hypertension or hypotension, tachycardia with rates up to 200 beats per minute, arrhythmias, nervousness, headache, tremor, dry mouth, palpitation, nausea, dizziness, fatigue, malaise, and insomnia.


Hypokalemia may also occur. As with all sympathomimetic medications, cardiac arrest and even death may be associated with abuse of PROVENTIL® HFA Inhalation Aerosol. Treatment consists of discontinuation of Proventil HFA Inhalation Aerosol together with appropriate symptomatic therapy. The judicious use of a cardioselective beta-receptor blocker may be considered, bearing in mind that such medication can produce bronchospasm. There is insufficient evidence to determine if dialysis is beneficial for overdosage of Proventil HFA Inhalation Aerosol.


The oral median lethal dose of albuterol sulfate in mice is greater than 2000 mg/kg (approximately 6800 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 3200 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). In mature rats, the subcutaneous median lethal dose of albuterol sulfate is approximately 450 mg/kg (approximately 3000 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 1400 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). In young rats, the subcutaneous median lethal dose is approximately 2000 mg/kg (approximately 14,000 times the maximum recommended daily inhalation dose for adults on a mg/m2 basis and approximately 6400 times the maximum recommended daily inhalation dose for children on a mg/m2 basis). The inhalation median lethal dose has not been determined in animals.



DOSAGE AND ADMINISTRATION


For treatment of acute episodes of bronchospasm or prevention of asthmatic symptoms, the usual dosage for adults and children 4 years of age and older is two inhalations repeated every 4 to 6 hours. More frequent administration or a larger number of inhalations is not recommended. In some patients, one inhalation every 4 hours may be sufficient. Each actuation of PROVENTIL® HFA Inhalation Aerosol delivers 108 mcg of albuterol sulfate (equivalent to 90 mcg of albuterol base) from the mouthpiece. It is recommended to prime the inhaler before using for the first time and in cases where the inhaler has not been used for more than 2 weeks by releasing four “test sprays” into the air, away from the face.



Exercise Induced Bronchospasm Prevention: The usual dosage for adults and children 4 years of age and older is two inhalations 15 to 30 minutes before exercise.


To maintain proper use of this product, it is important that the mouthpiece be washed and dried thoroughly at least once a week. The inhaler may cease to deliver medication if not properly cleaned and dried thoroughly (see PRECAUTIONS, Information for Patients section). Keeping the plastic mouthpiece clean is very important to prevent medication build-up and blockage. The inhaler may cease to deliver medication if not properly cleaned and air dried thoroughly. If the mouthpiece becomes blocked, washing the mouthpiece will remove the blockage.


If a previously effective dose regimen fails to provide the usual response, this may be a marker of destabilization of asthma and requires reevaluation of the patient and the treatment regimen, giving special consideration to the possible need for anti-inflammatory treatment, eg, corticosteroids.



HOW SUPPLIED


PROVENTIL® HFA (albuterol sulfate) Inhalation Aerosol is supplied as a pressurized aluminum canister with a yellow plastic actuator and orange dust cap each in boxes of one. Each actuation delivers 120 mcg of albuterol sulfate from the valve and 108 mcg of albuterol sulfate from the mouthpiece (equivalent to 90 mcg of albuterol base). Canisters with a labeled net weight of 6.7 g contain 200 inhalations (NDC 0085-1132-01).


Rx only. Store between 15°-25°C (59°-77°F). For best results, canister should be at room temperature before use.


SHAKE WELL BEFORE USING.


The yellow actuator supplied with Proventil HFA Inhalation Aerosol should not be used with any other product canister, and actuator from other products should not be used with a Proventil HFA Inhalation Aerosol canister. The correct amount of medication in each canister cannot be assured after 200 actuations, even though the canister is not completely empty. The canister should be discarded when the labeled number of actuations have been used.


WARNING: Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Exposure to temperatures above 120°F may cause bursting. Keep out of reach of children.


PROVENTI L ® HFA Inhalation Aerosol does not contain chlorfluorocarbons (CFCs) as the propellant.


Developed and Manufactured by

3M Health Care Limited

Loughborough UK


or


3M Drug Delivery Systems

Northridge, CA 91324


for


Schering Corporation,

a subsidiary of

Schering-Plough Corporation,

Kenilworth, NJ 07033 USA


Schering-Plough


© 1996, 1998, Schering Corporation.

All rights reserved.

The trademarks depicted in this piece are owned by their respective companies.


673700

Rev. 02/09



Attention Health Care Professional


Detach Patient's Instructions for Use from package insert and dispense with the product.


PROVENTIL® HFA


(albuterol sulfate)


Inhalation Aerosol


FOR ORAL INHALATION ONLY


Patient's Instructions for Use


Figure 1



Figure 2



Before using your PROVENTIL® HFA (albuterol Sulfate) Inhalation Aerosol, read complete instructions carefully. Children should use Proventil HFA Inhalation Aerosol under adult supervision, as instructed by the patient's doctor


Please note that


  1. SHAKE THE INHALER WELL immediately before each use. Then remove the cap from the mouthpiece (see Figure 1). Check mouthpiece for foreign objects prior to use. Make sure the canister is fully inserted into the actuator.

  2. As with all aerosol medications, it is recommended to prime the inhaler before using for the first time and in cases where the inhaler has not been used for more than 2 weeks. Prime by releasing four “test sprays” into the air, away from your face.

  3. BREATH OUT FULLY THROUGH THE MOUTH, expelling as much air from your lungs as possible. Place the mouthpiece fully into the mouth holding the inhaler in its upright position (see Figure 2) and closing the lips around it.

  4. WHILE BREATHING IN DEEPLY AND SLOWLY THROUGH THE MOUTH, FULLY DEPRESS THE TOP OF THE METAL CANISTER with your index finger (see Figure 2).

  5. HOLD YOUR BREATH AS LONG AS POSSIBLE, up to 10 seconds. Before breathing out, remove the inhaler from your mouth and release your finger from the canister.

  6. If your physician has prescribed additional puffs, wait 1 minute, shake the inhaler again, and repeat steps 3 through 5. Replace the cap after use.

  7. KEEPING THE PLACTIC MOUTHPIECE CLEAN IS EXTREMELY IMPORTANT TO PREVENT MEDICATION BUILD-UP AND BLOCKAGE. THE MOUTHPIECE SHOULD BE WASHED, SHAKEN TO REMOVE EXCESS WATER, AND AIR DRIED THOROUGHLY AT LEAST ONCE A WEEK. INHALER MAY STOP SPRAYING IF NOT PROPERLY CLEANED.
     

    Routine cleaning instructions:

     

    Step 1. To clean, remove the canister and mouthpiece cap. Wash the mouthpiece through the top and bottom with warm running water for 30 seconds at lease once a week (see Figure A). Never immerse the metal canister in water.

    Figure A



     

    Wash mouthpiece under warm running water.

    Figure B



     

    Allow mouthpiece to dry, such as overnight.

    Figure C



     

    When blocked, little or no medicine comes out.

     

    Step 2. To dry, shake off excess water and let the mouthpiece air dry thoroughly, such as overnight (see Figure B). When the mouthpiece is dry, replace the canister and the mouthpiece cap. Blockage from medication buildup is more likely to occur if the mouthpiece is not allowed to air dry thoroughly.

     

    IF YOUR INHALER HAS BECOME BLOCKED (little or no medication coming out of the mouthpiece, see Figure C), wash the mouthpiece as described in Step 1 and air dry thoroughly as described in Step 2.

     

    IF YOU NEED TO USE YOUR INHALER BEFORE IT IS COMPLETELY DRY, SHAKE OFF EXCESS WATER, replace the canister, and test spray twice into the air, away from your face, to remove most of the water remaining in the mouthpiece. Then take your dose as prescribed. After such use, rewash and air dry thoroughly as described in Step 1 and 2.


  8. The correct amount of medication in each inhalation cannot be assured after 200 actuations, even though the canister is not completely empty. The canister should be discarded when the labeled number of actuations have been used. Before you reach the specific number of actuations, you should consult your physician to determine whether a refill is needed. Just as you should not take extra doses without consulting your physician, you also should not stop using Proventil HFA Inhalation Aerosol without consulting your physician.

You may notice a slightly different taste or spray force than you are used to with Proventil HFA Inhalation Aerosol, compared to other albuterol inhalation aerosol products.


DOSAGE:


Use only as directed by your physician.


WARNINGS:


The action of PROVENTIL® HFA Inhalation Aerosol should last up to 4 to 6 hours. Proventil HFA Inhalation Aerosol should not be used more frequently than recommended. Do not increase the number of puffs or frequency of doses of Proventil HFA Inhalation Aerosol without consulting your physician. If you find that treatment with Proventil HFA Inhalation Aerosol becomes less effective for symptomatic relief, your symptoms become worse, and/or you need to use the product more frequently than usual, medical attention should be sought immediately. While you are taking Proventil HFA Inhalation Aerosol, other inhaled drugs should be taken only as directed by your physician. If you are pregnant or nursing, contact your physician about the use of Proventil HFA Inhalation Aerosol.


Common adverse effects of treatment with Proventil HFA Inhalation Aerosol include palpitations, chest pain, rapid heart rate, tremor, or nervousness. Effective and safe use of Proventil HFA Inhalation Aerosol includes an understanding of the way that it should be administered. Use Proventil HFA Inhalation Aerosol only with the yellow actuator supplied with the product. The Proventil HFA Inhalation Aerosol actuator should not be used with other aerosol medications.


For best results, use at room temperature. Avoid exposing product to extreme heat and cold.


Shake well before use.


Contents Under Pressure.


Do not puncture. Do not store near hear or open flame. Exposure to temperatures above 120°F may cause bursting. Never throw container into fire or incinerator. Store between 15° - 25°C (59° - 77°F). Avoid spraying in eyes. Keep out of reach of children.


Further Information: Your PROVENTIL® HFA (albuterol sulfate) Inhalation Aerosol does not contain chlorofluorocarbons (CFCs) as the propellant. Instead, the inhaler contains a hydrofluoroalkane (HFA-134a) as the propellant.


Developed and Manufactured by

3M Health Care Limited

Loughborough UK


or


3M Drug Delivery Systems

Northridge, CA 91324


For Schering Corporation

a subsidiary of

Schering-Plough Corporation,

Kenilworth, NJ 07033 USA


Schering-Plough


Rev. 02/09

673800


© 1996, 1999, Schering Corporation

All rights reserved.


U.S. Patent No. 5,225,183; 5,439,670; 5,605,674; 5,695,743; 5,766,573; and 6,352,684.



Principal Display Panel – USA Canister Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g




Principal Display Panel – USA Carton Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


CONTAINS NO


CHLOROFLUOROCARBONS




Principal Display Panel – Ireland Canister Label


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


Schering-Plough




Principal Display Panel – Ireland Carton Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


CONTAINS NO


CHLOROFLUOROCARBONS


Schering-Plough




Principal Display Panel – USA Canister Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g




Principal Display Panel – USA Carton Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


CONTAINS NO


CHLOROFLUOROCARBONS




Principal Display Panel – Ireland Canister Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g




Principal Display Panel – Ireland Carton Label


SCHERING


PROFESSIONAL SAMPLE NOT FOR SALE


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


100 METERED INHALATIONS


NET CONTENTS 3.7g


CONTAINS NO


CHLOROFLUOROCARBONS




Principal Display Panel – USA Canister Label


SCHERING


NDC 0085-1132-01


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


200 METERED INHALATIONS


NET CONTENTS 6.7g


Manufactured for Schering Corporation


Kenilworth, NJ 07033




Principal Display Panel – USA Carton Label


SCHERING


NDC 0085-1132-01


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


200 METERED INHALATIONS


NET CONTENTS 6.7g


CONTAINS NO


CHLOROFLUOROCARBONS




Principal Display Panel – Ireland Canister Label


NDC 0085-1132-01


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


200 METERED INHALATIONS


NET CONTENTS 6.7g


Mfd. for Schering Corp, a subsidiary


of Schering-Plough Corp.


Kenilworth, NJ 07033 USA


Schering-Plough




Principal Display Panel – Ireland Carton Label


NDC 0085-1132-01


PROVENTIL ® HFA


(Albuterol Sulfate Inhalation Aerosol)


FOR ORAL INHALATION WITH


PROVENTIL ® HFA ACTUATOR ONLY


Rx only


200 METERED INHALATIONS


NET CONTENTS 6.7g


CONTAINS NO


CHLOROFLUOROCARBONS


Schering-Plough




Principal Display Panel – USA Canister Label


SCHERING


NDC 0085-1132-01