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Drug Information for Fluoxetine Hydrochloride (Northstar Rx LLC): ANIMAL PHARMACOLOGY/TOXICOLOGY
- BOXED WARNING
- DESCRIPTION
- CLINICAL TRIALS
- INDICATIONS AND USAGE
- CONTRAINDICATIONS
- WARNINGS
- ADVERSE REACTIONS
- DRUG ABUSE AND DEPENDENCE
- OVERDOSAGE
- DOSAGE AND ADMINISTRATION
- HOW SUPPLIED
- ANIMAL PHARMACOLOGY/TOXICOLOGY
- Medication Guide
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 10 mg (30 count)
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 10 mg (100 count)
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 10 mg (1000 count)
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 20 mg (30 count)
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 20 mg (100 count)
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 20 mg (1000 count)
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 40 mg (30 count)
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 40 mg (100 count)
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 40 mg (500 count)
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - 40 mg (1000 count)
- External Links Related to Fluoxetine Hydrochloride (Northstar Rx LLC)
- Phospholipids are increased in some tissues of mice, rats, and dogs given fluoxetine chronically. This effect is reversible after cessation of fluoxetine treatment. Phospholipid accumulation in animals has been observed with many cationic amphiphilic drugs, including fenfluramine, imipramine, and ranitidine. The significance of this effect in humans is unknown.
- Drug Information Provided by National Library of Medicine (NLM).