Naproxen description, usages, side effects, indications, overdosage, supplying and lots more!

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Naproxen

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

BOXED WARNING

Cardiovascular Risk
WARNINGS).
WARNINGS).
Gastrointestinal Risk
WARNINGS).

NAPROXEN DESCRIPTION



Naproxen




CLINICAL PHARMACOLOGY

Pharmacodynamics

Pharmacokinetics

Absorption



PRECAUTIONS: Nursing Mothers).



WARNINGS: Renal Effects).








WARNINGS: Renal Effects).

CLINICAL STUDIES

General Information









Geriatric Patients

INDICATIONS & USAGE

WARNINGS).










NAPROXEN CONTRAINDICATIONS


WARNINGS: Anaphylactoid ReactionsandPRECAUTIONS: Preexisting Asthma).
WARNINGS).

WARNINGS

CARDIOVASCULAR EFFECTS


Gastrointestinal Effects - Risk of Ulceration, Bleeding, and Perforation).
CONTRAINDICATIONS).




Gastrointestinal Effects- Risk of Ulceration, Bleeding, and Perforation



Renal Effects
WARNINGS: Advanced Renal Disease).
Advanced Renal Disease

Anaphylactoid Reactions
CONTRAINDICATIONSandPRECAUTIONS: Preexisting Asthma). Emergency help should be sought in cases where an anaphylactoid reaction occurs.
Skin Reactions

Pregnancy

PRECAUTIONS

General
Naproxen-containing products such as Naproxen Tablets, USP, and other naproxen products should not be used concomitantly since they all circulate in the plasma as the naproxen anion.




Hepatic Effects




Hematological Effects


Preexisting Asthma

INFORMATION FOR PATIENTS

Patients should be informed of the following information before initiating therapy with an NSAID and periodically during the course of ongoing therapy. Patients should also be encouraged to read the NSAID Medication Guide that accompanies each prescription dispensed.
WARNINGS: Cardiovascular Effects).
WARNINGS: Gastrointestinal Effects- Risk of Ulceration, Bleeding, and Perforation).



WARNINGS).


LABORATORY TESTS


DRUG INTERACTIONS










WARNINGS: Renal Effects), as well as to assure diuretic efficacy.






Other Information Concerning Drug Interactions
Naproxen is highly bound to plasma albumin; it thus has a theoretical potential for interaction with other albumin-bound drugs such as coumarin-type anticoagulants, sulphonylureas, hydantoins, other NSAIDs, and aspirin. Patients simultaneously receiving naproxen and a hydantoin, sulphonamide or sulphonylurea should be observed for adjustment of dose if required.



DRUG & OR LABORATORY TEST INTERACTIONS




CARCINOGENESIS


PREGNANCY






LABOR & DELIVERY


NURSING MOTHERS


PEDIATRIC USE


GERIATRIC USE


WARNINGS).
WARNINGS: Renal Effects).

NAPROXEN ADVERSE REACTIONS


CLINICAL PHARMACOLOGY).


Gastrointestinal (GI) Experiences, including:heartburn1, abdominal pain1, nausea1, constipation1, diarrhea, dyspepsia, and stomatitis
Central Nervous System:headache1, dizziness1, drowsiness1, lightheadedness, vertigo
Dermatologic:pruritus (itching)1, skin eruptions1, ecchymoses1, sweating, purpura
Special Senses:tinnitus1, visual disturbances, hearing disturbances
Cardiovascular:edema1, palpitations.
General:dyspnea1, thirst




Body as a Whole:anaphylactoid reactions, angioneurotic edema, menstrual disorders, pyrexia (chills and fever)
Cardiovascular:congestive heart failure, vasculitis, hypertension, pulmonary edema
Gastrointestinal:gastrointestinal bleeding and/or perforation, hematemesis, pancreatitis, vomiting, colitis, nonpeptic gastrointestinal ulceration, ulcerative stomatitis, peptic ulceration
Hepatobiliary:jaundice, abnormal liver function tests, hepatitis (some cases have been fatal)
Hemic and Lymphatic:eosinophilia, leucopenia, melena, thrombocytopenia, agranulocytosis, granulocytopenia, hemolytic anemia, aplastic anemia
Metabolic and Nutritional:hyperglycemia, hypoglycemia
Nervous System:inability to concentrate, depression, dream abnormalities, insomnia, malaise, myalgia, muscle weakness, aseptic meningitis, cognitive dysfunction, convulsions
Respiratory:eosinophilic pneumonitis, asthma
Dermatologic:alopecia, urticaria, skin rashes, toxic epidermal necrolysis, erythemia multiforme, erythema nodosum, fixed drug eruption, lichen planus, pustular reaction, systemic lupus erythematosus, Stevens-Johnson syndrome, photosensitive dermatitis, photosensitivity reactions, including rare cases resembling porphyria cutanea tarda (pseudoporphyria) or epidermolysis bullosa. If skin fragility, blistering or other symptoms suggestive of pseudoporphyria occur, treatment should be discontinued and the patient monitored.
Special Senses:hearing impairment, corneal opacity, papillitis, retrobulbar optic neuritis, papilledema
Urogenital:glomerular nephritis, hematuria, hyperkalemia, interstitial nephritis, nephrotic syndrome, renal disease, renal failure, renal papillary necrosis, raised serum creatinine
Reproduction (female):infertility

Body as a Whole:fever infection, sepsis, anaphylactic reactions, appetite changes, death
Cardiovascular:hypertension, tachycardia, syncope, arrhythmia, hypotension, myocardial infarction
Gastrointestinal:dry mouth, esophagitis, gastric/peptic ulcers, gastritis, glossitis, eructation
Hepatobiliary:hepatitis, liver failure
Hemic and Lymphatic:rectal bleeding, lymphadenopathy, pancytopenia
Metabolic and Nutritional:weight changes
Nervous System:anxiety, asthenia, confusion, nervousness, paresthesia, somnolence, tremors, convulsions, coma, hallucinations
Respiratory:asthma, respiratory depression, pneumonia
Dermatologic:exfoliative dermatitis
Special Senses:blurred vision, conjunctivitis
Urogenital:cystitis, dysuria, oliguria/polyuria, proteinuria

OVERDOSAGE



DOSAGE & ADMINISTRATION

WARNINGS).

Different dose strengths and formulations (i.e., tablets, suspension) of the drug are not necessarily bioequivalent. This difference should be taken into consideration when changing formulation.

WARNINGSandPRECAUTIONS).
Geriatric Patients

Patients With Moderate to Severe Renal Impairment
WARNINGS: Renal Effects).
Rheumatoid Arthritis, Osteoarthritis and Ankylosing Spondylitis

CLINICAL PHARMACOLOGY).
Acute Gout

HOW SUPPLIED

Naproxen Tablets, USP:
250 mg:white, round, biconvex, debossed with188on obverse andon the reverse. Packaged in bottles of 100, 500 and 1000.
375 mg:white, capsule-shaped, biconvex, debossed with189on obverse andon the reverse. Packaged in bottles of 100, 500 and 1000.
500 mg:white, capsule-shaped, biconvex, debossed with190on obverse andon the reverse. Packaged in bottles of 100, 500 and 1000.

STORAGE AND HANDLING


SPL MEDGUIDE

Medication Guide
for
Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)

What is the most important information I should know about medicines called
Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)?
NSAID medicines may increase the chance of a heart attack or stroke that can lead to death.This chance increases:
NSAID medicines should never be used right before or after a heart surgery called a
artery bypass graft (CABG).
NSAID medicines can cause ulcers and bleeding in the stomach and intestines at any
time during treatment. Ulcers and bleeding:
The chance of a person getting an ulcer or bleeding increases with:

NSAID medicines should only be used:
What are Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)?



Who should not take a Non-Steroidal Anti-Inflammatory Drug (NSAID)?
Do not take an NSAID medicine:


Tell your healthcare provider:

Keep a list of your medicines to show to your healthcare provider and pharmacist.
NSAID medicines should not be used by pregnant women late in their pregnancy.
Talk to your doctor.
What are the possible side effects of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)?
Serious side effects include: Other side effects include:
















Get emergency help right away if you have any of the following symptoms:
Stop your NSAID medicine and call your healthcare provider right away if you have any of the following symptoms:

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Other information about Non-Steroidal Anti-Inflammatory Drugs (NSAIDs)


NSAID medicines that need a prescription
Generic Name Tradename

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Naproxen


Naproxen

Naproxen

NAPROXEN TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:49349-712(NDC:53746-190)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Naproxen NAPROXEN 500 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
povidone
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
white 16 mm IP190;500 BULLET

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49349-712-10 6 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075927 2012-09-04


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Be sure to consult your doctor before taking any medication!
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