Sunday 28 February 2010

Reserpine




In some countries, this medicine may only be approved for veterinary use.


In the US, Reserpine (reserpine systemic) is a member of the drug class antiadrenergic agents, peripherally acting and is used to treat High Blood Pressure, Hyperthyroidism and Schizophrenia.

US matches:

  • Reserpine

  • Reserpine, hydralazine, and hydrochlorothiazide

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

C02AA02

CAS registry number (Chemical Abstracts Service)

0000050-55-5

Chemical Formula

C33-H40-N2-O9

Molecular Weight

608

Therapeutic Category

Antihypertensive agent

Chemical Name

Yohimban-16-carboxylic acid, 11,17-dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-, methyl ester, (3ß,16ß,17α,18ß,20α)-

Foreign Names

  • Reserpinum (Latin)
  • Reserpin (German)
  • Réserpine (French)
  • Reserpina (Spanish)

Generic Names

  • Reserpina (OS: DCIT)
  • Reserpine (OS: JAN, BAN)
  • Réserpine (OS: DCF)
  • Mephaserpin (IS)
  • Reserpin (PH: Ph. Eur. 6)
  • Reserpine (PH: BP 2010, JP XIV, Ph. Int. 4, USP 32, Ph. Eur. 6)
  • Réserpine (PH: Ph. Eur. 6)
  • Reserpinum (PH: Ph. Int. 4, Ph. Eur. 6)

Brand Names

  • Adelphane Esidrex (Reserpine and Dihydralazine, + Hydrochlorothiazide)
    Novartis, Bahrain


  • Apoplon
    Daiichi Sankyo, Japan


  • Behyd RA (Reserpine and Benzylhydrochlorothiazide)
    Kyorin, Japan


  • Brinerdin (Reserpine and Clopamide, + Dihydroergocristine)
    Krka, Slovenia; Novartis, Bahrain; Novartis, Switzerland; Novartis, Oman; Novartis, South Africa


  • Briserin (Reserpine and Clopamide)
    Novartis, Germany


  • Hygroton-Reseprine (Reserpine and Chlortalidone)
    Novartis, Greece


  • Hygroton-Reserpin (Reserpine and Chlortalidone)
    Novartis, Switzerland


  • Igroton Reserpina (Reserpine and Chlortalidone)
    Novartis, Italy


  • Neourizine (Reserpine and Chlorothiazide)
    Adelco, Greece


  • Rakelin (veterinary use)
    Nature Vet, Australia; Vetpharm, New Zealand


  • Regroton (Reserpine and Chlortalidone)
    Novartis, Turkey


  • Reserpine
    Aspen Pharmacare, South Africa; Eon, United States; Sandoz, United States


  • Rethizid (Reserpine andHydrochlorothiazide)
    Balkanpharma, Bulgaria


  • Serpalan
    Lannett, United States


  • Serpasil
    Biochemie, Indonesia; Novartis, Ethiopia


  • Triniton (Reserpine and Dihydralazine, + Hydrochlorothiazide)
    Apogepha, Germany

International Drug Name Search

Glossary

BANBritish Approved Name
DCFDénomination Commune Française
DCITDenominazione Comune Italiana
ISInofficial Synonym
JANJapanese Accepted Name
OSOfficial Synonym
PHPharmacopoeia Name
Rec.INNRecommended International Nonproprietary Name (World Health Organization)

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

Bovilactoplex




Bovilactoplex may be available in the countries listed below.


In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Bovilactoplex



Oxytetracycline

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


  • Austria

Tylosin

Tylosin tartrate (a derivative of Tylosin) is reported as an ingredient of Bovilactoplex in the following countries:


  • Austria

International Drug Name Search

Saturday 27 February 2010

Pergolide PCH




Pergolide PCH may be available in the countries listed below.


Ingredient matches for Pergolide PCH



Pergolide

Pergolide mesilate (a derivative of Pergolide) is reported as an ingredient of Pergolide PCH in the following countries:


  • Netherlands

International Drug Name Search

Wednesday 24 February 2010

Ranopril




Ranopril may be available in the countries listed below.


Ingredient matches for Ranopril



Lisinopril

Lisinopril is reported as an ingredient of Ranopril in the following countries:


  • Poland

International Drug Name Search

Thursday 18 February 2010

Doxycycline Hyclate eent


Class: Antibacterials
Chemical Name: 4 - (Dimethylamino) - 1,4,4a,5,5a,6,11,12a - octahydro - 3,5,10,12,12a - pentahydroxy - 6 - methyl - 1,11 - dioxo - 2 - naphthacenecarboxamide monohydrochloride
Molecular Formula: (C22H24N2O8•HCl)2
CAS Number: 24390-14-5
Brands: Atridox, Periostat

Introduction

Semisynthetic tetracycline antibiotic.1


Uses for Doxycycline Hyclate


Periodontitis


Used orally as an adjunct to scaling and root planing to promote attachment-level gain and to reduce pocket depth in adults with periodontitis.14 15 16


Used subgingivally in treatment of chronic periodontitis in adults to reduce pocket depth, gain clinical attachment level, and reduce bleeding associated with probing.1 2 3 4 5 7 10 11


Doxycycline Hyclate Dosage and Administration


Administration


Oral Administration


Administered orally as 20-mg tablets for adjunctive treatment of periodontitis.14


Administer doses in the morning and evening and at least 1 hour prior to or 2 hours after meals.14


Give with adequate amounts of fluids to reduce risk of esophageal irritation and ulceration.14


Subgingival Administration


Administered subgingivally (as an extended-release preparation containing the drug incorporated into a bioresorbable polymer) into periodontal pockets by an oral health-care professional.1 4 10 11


Each pair of syringes is intended for single use only.1


Administration does not require local anesthesia.1


Preparation does not have to be manually removed; preparation solidifies upon contact with gingival crevicular fluid and is bioabsorbed or expelled naturally.1


Reconstitution

Mix contents of the 2 paired syringes (liquid polymeric delivery system [syringe A]; doxycycline hyclate powder [syringe B]) together prior to administration.1 Remove syringes from the refrigerator at least 15 minutes prior to mixing.1


Couple syringes together and inject contents of syringe A into syringe B and then back into syringe A to complete 1 mixing cycle.1 Perform 100 mixing cycles (approximately 1 mixing cycle per second) prior to administration.1


If not administered immediately, store coupled syringes in resealable pouch at room temperature for up to 3 days; an additional 10 mixing cycles is required just prior to administration.1


After mixing, hold coupled syringes vertically with syringe A (indicated by a purple stripe) at the bottom.1 Pull down on the plunger of syringe A and allow contents to flow down the barrel for several seconds into syringe A.1 Uncouple syringes and attach the blunt cannula supplied in the package to syringe A prior to administration.1 Bend cannula to resemble a periodontal probe.1


Subgingival Administration Technique

Using the syringe with bent cannula, position tip of cannula near the base of the periodontal pocket and administer preparation into the pocket until the formulation reaches the top of the gingival margin.1


After administration is completed, withdraw cannula from the pocket and cover pocket with periodontal dressing or dental adhesive.1


Dosage


Available as doxycycline hyclate; dosage expressed in terms of doxycycline; 50 mg of doxycycline hyclate equivalent to 42.5 mg of doxycycline.1


Adults


Periodontitis

Oral

20 mg every 12 hours.14


Safety of >12 months of treatment and efficacy of >9 months of treatment have not been established.14


Subgingival

Dosage varies depending on the size, shape, and number of periodontal pockets treated.1 May repeat treatment 4 months after the initial treatment.1


Cautions for Doxycycline Hyclate


Contraindications



  • Known hypersensitivity to doxycycline or other tetracyclines.1 14



Warnings/Precautions


Warnings


Dental and Bone Effects

Avoid use during tooth development (e.g., the last half of pregnancy, infancy, childhood up to 8 years of age); potential for permanent tooth discoloration or enamel hypoplasia.1 14


Tetracyclines form a stable calcium complex in any bone-forming tissue.14 Reversible decrease in fibula growth rate has occurred in premature infants receiving oral tetracycline.14


Sensitivity Reactions


Photosensitivity Reactions

Possible photosensitivity reactions (e.g., exaggerated sunburn reaction).1 14 Discontinue oral or subgingival therapy at the first sign of skin erythema.13 14


General Precautions


Precautions Related to Subgingival Doxycycline

Not studied for use in the regeneration of alveolar bone, either in preparation for or in conjunction with placement of endosseous (dental) implants or in the treatment of failing implants.1


Not studied in patients with extremely severe periodontal defects with little remaining periodontium.1


Not studied in immunocompromised patients (e.g., those with diabetes or HIV infection, those receiving chemotherapy or radiation therapy).1


Oral Candidiasis

Possible overgrowth of nonsusceptible organisms, including fungi.1 14 Use with caution in patients with a history of or predisposition to oral candidiasis.1 14 Safety and efficacy not established in patients with concomitant oral candidiasis.1 14


Specific Populations


Pregnancy

Category D.1 14


Lactation

Distributed into milk.1 14 Discontinue nursing or the drug.1 14


Pediatric Use

Do not use oral doxycycline in children <8 years of age.14


Safety and efficacy of subgingival doxycycline not established in children <18 years of age.1 2 13


Possible permanent tooth discoloration (see Dental and Bone Effects under Cautions).1


Common Adverse Effects


Oral: Headache, common cold, flu symptoms, toothache, GI symptoms (diarrhea, nausea, dyspepsia), joint pain.14


Subgingival: Headache; common cold; gum discomfort, pain or soreness, loss of attachment, or increased pocket depth; toothache or pressure sensitivity; periodontal abscess, exudate, infection, drainage, extreme mobility, or suppuration; thermal tooth sensitivity.1


Interactions for Doxycycline Hyclate


Drug interactions reported involve oral doxycycline.14 No formal drug interaction studies have been performed with doxycycline hyclate polymer for subgingival administration.1


Specific Drugs






























Drug



Interaction



Comments



Antacids (aluminum-, calcium-, or magnesium-containing)



Decreased doxycycline absorption14



Anticoagulants, oral



Possible decreased prothrombin activity14



Adjust anticoagulant dosage as needed14



Anticonvulsants (barbiturates, carbamazepine, phenytoin)



Possible decreased doxycycline half-life14



Bismuth subsalicylate



Possible decreased doxycycline absorption14



Hormonal contraceptives



Possible decreased effectiveness of oral contraceptives1 14



Iron-containing preparations



Possible decreased doxycycline absorption14



Methoxyflurane



Fatal renal toxicity reported with concomitant use of tetracycline and methoxyflurane14



Penicillins



Possible antagonism14



Avoid concomitant use14


Doxycycline Hyclate Pharmacokinetics


Absorption


Bioavailability


Oral: Doxycycline hyclate rapidly and almost completely absorbed from GI tract.14 In adults receiving 20-mg tablets of doxycycline hyclate, peak serum doxycycline concentrations attained within 1.4 hours after a single dose or within 2 hours of a dose at steady-state.14


Subgingival: Concentrations in gingival crevicular fluid (GCF) peaked 2 hours following administration and remained >1000 mcg/mL through 18 hours.1 GCF concentrations then declined gradually but remained >MIC for periodontal pathogens (≤6 mcg/mL) through 7 days; serum concentrations remained ≤0.1 mcg/mL.1


Stability


Storage


Oral


Tablets

15–30°C in tight, light-resistant container.14


Subgingival


For liquid, extended-release polymer

2–8°C.1


Actions and SpectrumActions



  • Usually is bacteriostatic.1




  • Inhibits protein synthesis in susceptible organisms.1




  • Active in vitro at concentrations of ≤6 mcg/mL against Porphyromonas gingivalis, Prevotella intermedia, Campylobacter rectus, and Fusobacterium nucleatum.1




  • No evidence of doxycycline or multidrug resistance in subgingival plaque or saliva in a clinical study of 6 months’ duration of subgingival doxycycline hyclate.1 6



Advice to Patients



  • When taking doxycycline hyclate tablets, importance of drinking sufficient amounts of fluids to reduce the risk of esophageal irritation and ulceration.14




  • Doxycycline hyclate polymer for subgingival administration is not meant for self-administration; only qualified oral health-care professionals familiar with administration of the subgingival preparation should administer the drug.1




  • Importance of not using mechanical oral hygiene procedures (i.e., brushing teeth, flossing) for 7 days following administration of the subgingival preparation.1




  • Importance of avoiding exposure to direct sunlight or UV light while receiving oral or subgingival doxycycline hyclate; importance of notifying clinician and of discontinuing therapy at the first sign of skin erythema.1 13




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




  • Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant diseases.1




  • Importance of informing 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.


* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name























Doxycycline Hyclate

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Oral



Tablets



20 mg (of doxycycline)



Periostat



CollaGenex



Tablets, film-coated



20 mg (of doxycycline)*



Doxycycline Hyclate Tablets



Teva



Subgingival



For liquid, extended-release polymer



10% w/w (to deliver 42.5 mg [of doxycycline])



Atridox (available in a 2-syringe Atrigel Delivery System)



CollaGenex



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 June 2006. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.




References



1. CollaGenex Pharmaceuticals. Atridox (doxycycline hyclate 10%) prescribing information. Newtown, PA; 1998 Sep.



2. Wennström JL, Newman HN, MacNeill SR et al. Utilisation of locally delivered doxycycline in non-surgical treatment of chronic periodontitis. J Clin Periodontol. 2001; 28:753-761.



3. Garrett S, Adams DF, Bogle G et al. The effect of locally delivered controlled-release doxycycline or scaling and root planing on periodontal maintenance patients over 9 months. J Periodontol. 2000; 71:22-30. [PubMed 10695935]



4. Garrett S, Johnson L, Drisko CH et al. Two multi-center studies evaluating locally delivered doxycycline hyclate, placebo control, oral hygiene, and scaling and root planing in the treatment of periodontitis. J Periodontol. 1999; 70:490-503. [PubMed 10368053]



5. Drisko CH. The use of locally-delivered doxycycline in the treatment of periodontitis. Clinical results. J Clin Periodontol. 1998; 25:947-52. [PubMed 9839851]



6. Walker CB, Godowski KC, Borden L. The effects of sustained release doxycycline on anaerobic flora and antibiotic-resistant patterns in subgingival plaque and saliva. J Periodontol. 2000; 71:768-74. [PubMed 10872958]



7. Wolinsky LE, Camargo PM, Polson A et al. The significance of prior mechanical therapy for changes of periodontal status achieved by local delivery of a doxycycline-hyclate containing gel. J Clin Periodontol. 2001; 28:1115-20. [PubMed 11737508]



8. Stoller NH, Johnson LR, Trapnell S et al. The pharmacokinetic profile of a biodegradable controlled-release delivery system containing doxycycline compared to systemically delivered doxycycline in gingival crevicular fluid, saliva, and serum. J Periodontol. 1998; 69:1085-91. [PubMed 9802705]



9. Ryder MI, Pons B, Adams D et al. Effects of smoking on local delivery of controlled-release doxycycline as compared to scaling and root planing. J Clin Periodontol. 1999; 26:683-91. [PubMed 10522780]



10. Greenstein G, Tonetti M and the Research, Science, and Therapy Committee of the American Academy of Periodontology. Position Paper. The role of controlled drug delivery for periodontitis. J Periodontol. 2000; 71:125-40. [PubMed 10695948]



11. Greenstein G, Polson A. The role of local drug delivery in the management of periodontal diseases: a comprehensive review. J Periodontol. 1998; 69:507-520. [PubMed 9623893]



12. Garrett S. Local delivery of doxycycline for the treatment of periodontitis. Compendium. 1999; 20:437-46. [PubMed 10650359]



13. CollaGenex Pharmaceuticals, Inc. Newtown, PA; Personal communication.



14. CollaGenex Pharmaceuticals. Periostat (doxycycline hyclate) 20 mg tablets prescribing information. Newtown, PA; 2003 Oct.



15. Greenstein G. The role of Periostat in the management of adult periodontitis: a critical assessment. Compend Contin Educ Dent. 1999; 20:664,666-8,670,672,574,676-8. [PubMed 10650384]



16. Caton JG. Evaluation of Periostat for patient management. Compend Contin Educ Dent. 1999; 20:451-2,454-6,458-63. [PubMed 10650360]



More Doxycycline Hyclate eent resources


  • Doxycycline Hyclate eent Use in Pregnancy & Breastfeeding
  • Drug Images
  • Doxycycline Hyclate eent Drug Interactions
  • Doxycycline Hyclate eent Support Group
  • 153 Reviews for Doxycycline Hyclate eent - Add your own review/rating


Compare Doxycycline Hyclate eent with other medications


  • Acne
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  • Amebiasis
  • Anthrax
  • Anthrax Prophylaxis
  • Bacterial Infection
  • Bartonellosis
  • Bronchitis
  • Brucellosis
  • Bullous Pemphigoid
  • Chlamydia Infection
  • Cholera
  • Cutaneous Bacillus anthracis
  • Ehrlichiosis
  • Enterocolitis
  • Epididymitis, Sexually Transmitted
  • Gastroenteritis
  • Granuloma Inguinale
  • Inclusion Conjunctivitis
  • Lyme Disease
  • Lyme Disease, Arthritis
  • Lyme Disease, Carditis
  • Lyme Disease, Erythema Chronicum Migrans
  • Lyme Disease, Neurologic
  • Lymphogranuloma Venereum
  • Malaria
  • Malaria Prevention
  • Melioidosis
  • Mycoplasma Pneumonia
  • Nongonococcal Urethritis
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  • Pelvic Inflammatory Disease
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  • Pleural Effusion
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  • Rabbit Fever
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  • Rickettsial Infection
  • Rosacea
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  • STD Prophylaxis
  • Syphilis, Early
  • Syphilis, Latent
  • Tertiary Syphilis
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Sunday 14 February 2010

MST Continus




MST Continus may be available in the countries listed below.


UK matches:

  • MST Continus suspensions 20, 30, 60, 100 and 200 mg
  • MST Continus tablets 5 mg, 10 mg, 15 mg, 30 mg, 60 mg, 100 mg, 200 mg
  • MST Continus suspensions 20, 30, 60, 100 and 200 mg (SPC)
  • MST Continus tablets 5 mg, 10 mg, 15 mg, 30 mg, 60 mg, 100 mg, 200 mg (SPC)

Ingredient matches for MST Continus



Morphine

Morphine sulphate pentahydrate (a derivative of Morphine) is reported as an ingredient of MST Continus in the following countries:


  • Argentina

  • Croatia (Hrvatska)

  • Czech Republic

  • Estonia

  • Germany

  • Hong Kong

  • Hungary

  • Indonesia

  • Ireland

  • Malta

  • Philippines

  • Poland

  • Romania

  • Singapore

  • Slovakia

  • Slovenia

  • South Africa

  • Spain

  • Switzerland

  • Taiwan

  • United Kingdom

International Drug Name Search

Glossary

SPC Summary of Product Characteristics (UK)

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

Thursday 11 February 2010

Levozine




Levozine may be available in the countries listed below.


Ingredient matches for Levozine



Levofloxacin

Levofloxacin is reported as an ingredient of Levozine in the following countries:


  • Peru

International Drug Name Search

Céfamandole




Céfamandole may be available in the countries listed below.


Ingredient matches for Céfamandole



Cefamandole

Céfamandole (DCF) is known as Cefamandole in the US.

International Drug Name Search

Glossary

DCFDénomination Commune Française

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

Wednesday 10 February 2010

Normosang




Normosang may be available in the countries listed below.


Ingredient matches for Normosang



Hemin

Hemin is reported as an ingredient of Normosang in the following countries:


  • Belgium

  • France

  • Netherlands

  • Sweden

Hemin Heme arginate (a derivative of Hemin) is reported as an ingredient of Normosang in the following countries:


  • Austria

  • Denmark

  • Estonia

  • Germany

  • Italy

  • Malta

  • Spain

  • Switzerland

International Drug Name Search

Peptulan




Peptulan may be available in the countries listed below.


Ingredient matches for Peptulan



Bismuthate, Tripotassium Dicitrato-

Bismuthate, Tripotassium Dicitrato- is reported as an ingredient of Peptulan in the following countries:


  • Brazil

International Drug Name Search

Monday 8 February 2010

Ambrex




Ambrex may be available in the countries listed below.


Ingredient matches for Ambrex



Ambroxol

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


  • Bulgaria

International Drug Name Search

Urutal




Urutal may be available in the countries listed below.


Ingredient matches for Urutal



Betahistine

Betahistine dihydrochloride (a derivative of Betahistine) is reported as an ingredient of Urutal in the following countries:


  • Bosnia & Herzegowina

  • Croatia (Hrvatska)

  • Serbia

  • Slovenia

International Drug Name Search

Sunday 7 February 2010

Orphenate


Generic Name: orphenadrine (Injection route)

or-FEN-a-dreen

Commonly used brand name(s)

In the U.S.


  • Antiflex

  • Mio-Rel

  • Norflex

  • Orfro

  • Orphenate

Available Dosage Forms:


  • Solution

Therapeutic Class: Skeletal Muscle Relaxant, Centrally Acting


Pharmacologic Class: Antimuscarinic


Uses For Orphenate


Orphenadrine is used to help relax certain muscles in your body and relieve the stiffness, pain, and discomfort caused by strains, sprains, or other injury to your muscles. However, this medicine does not take the place of rest, exercise or physical therapy, or other treatment that your doctor may recommend for your medical problem .


Orphenadrine acts in the central nervous system (CNS) to produce its muscle relaxant effects .


This medicine is available only with your doctor's prescription .


Before Using Orphenate


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


Pediatric


Appropriate studies have not been performed on the relationship of age to the effects of orphenadrine in the pediatric population. Safety and efficacy have not been established .


Geriatric


No information is available on the relationship of age to the effects of orphenadrine in geriatric patients. However, elderly patients are more likely to have age-related heart, liver, or kidney problems which may require caution in patients receiving orphenadrine .


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are receiving this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Perphenazine

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Enlarged esophagus or

  • Enlarged prostate or

  • Glaucoma or

  • Intestinal blockage or

  • Myasthenia gravis or

  • Stomach ulcer or

  • Urinary tract blockage—Orphenadrine should not be used in patients with these conditions .

  • Heart problems (e.g., fast or irregular heartbeats, heart failure)—Use with caution. Orphenadrine may worsen these conditions .

Proper Use of orphenadrine

This section provides information on the proper use of a number of products that contain orphenadrine. It may not be specific to Orphenate. Please read with care.


A nurse or other trained health professional will give you this medicine. This medicine is given through a needle placed in one of your veins or into your muscle .


Precautions While Using Orphenate


Your doctor will only give you a few doses of this medicine until your condition improves, and then you will be switched to an oral medicine that works the same way. If you have any concerns about this, talk to your doctor .


Orphenate Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor or nurse immediately if any of the following side effects occur:


Rare
  • Cough

  • difficulty swallowing

  • dizziness

  • fast heartbeat

  • hives

  • itching

  • puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue

  • shortness of breath

  • skin rash

  • tightness in chest

  • unusual tiredness or weakness

  • wheezing

Incidence not known
  • Abdominal or stomach pain

  • diarrhea

  • fast, pounding, or irregular heartbeat or pulse

  • fever

  • glaucoma

  • joint or muscle pain

  • nausea

  • numbness or tingling of face, hands, or feet

  • redness and soreness of eyes

  • shortness of breath

  • sores in mouth

  • swelling of feet or lower legs

  • vomiting

Get emergency help immediately if any of the following symptoms of overdose occur:


Symptoms of Overdose
  • Blurred vision

  • confusion, delirium, or hallucinations

  • constipation

  • difficult urination

  • drowsiness

  • dry eyes, mouth, nose, or throat

  • eye pain

  • flushing or redness of face

  • troubled breathing

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


Incidence not known
  • Anxiety

  • deep or fast breathing with dizziness

  • headache

  • irritability

  • itching skin

  • mental confusion

  • nervousness

  • numbness of feet, hands and around mouth

  • restlessness

  • trembling or shaking of hands or feet shakiness in legs, arms, hands, or feet

  • unusually large pupils of eyes

  • weakness

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Orphenate side effects (in more detail)



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More Orphenate resources


  • Orphenate Side Effects (in more detail)
  • Orphenate Use in Pregnancy & Breastfeeding
  • Orphenate Drug Interactions
  • Orphenate Support Group
  • 0 Reviews for Orphenate - Add your own review/rating


  • Norflex Prescribing Information (FDA)

  • Norflex Concise Consumer Information (Cerner Multum)

  • Norflex Monograph (AHFS DI)

  • Norflex MedFacts Consumer Leaflet (Wolters Kluwer)



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