Brand Name: Luvox
Outside U.S., Brand Names also known as: Dumirox; Dumyrox; Faverin; Favoxil;
Fevarin; Floxyfral; Maveral
Fluvoxamine is used to treat obsessive-compulsive disorder, OCD, and treat depression. Detailed info on uses, dosage and side-effects of Fluvoxamine below.
Contents:
Description
Pharmacology
Indications and Usage
Contraindications
Warnings
Precautions
Drug Interactions
Adverse Reactions
Overdose
Dosage
Supplied
Fluvoxamine (Luvox) is a selective serotonin reuptake inhibitor (SSRI) used to
treat obsessive-compulsive disorder (OCD). It may also be used to treat
depression and other conditions as determined by your doctor.
The mechanism of action of fluvoxamine maleate in Obsessive Compulsive Disorder
is presumed to be linked to its specific serotonin reuptake inhibition in brain
neurons. In preclinical studies, it was found that fluvoxamine inhibited
neuronal uptake of serotonin.
Following a single 100 mg oral dose, peak plasma levels of 31 to 87 ng/mL were
attained 1.5 to 8 hours post-dose.
Luvox (Fluvoxamine Maleate) is indicated for the treatment of obsessions and
compulsions in patients with Obsessive Compulsive Disorder (OCD).
Obsessive Compulsive Disorder is characterized by recurrent and persistent
ideas, thoughts, impulses or images (obsessions) that are ego-dystonic and/or
repetitive, purposeful, and intentional behaviors (compulsions) that are
recognized by the person as excessive or unreasonable.
For the symptomatic relief of depressive illness.
The effectiveness of fluvoxamine maleate for long-term use, i.e., for more than
10 weeks, has not been systematically evaluated in placebo-controlled trials.
Therefore, the physician who elects to use fluvoxamine maleate for extended
periods should periodically re-evaluate the long-term usefulness of the drug for
the individual patient.
Co-administration of terfenadine (Seldane), astemizole (Hismanal), or cisapride
with fluvoxamine maleate is contraindicated.
Fluvoxamine maleate are contraindicated in patients with a history of
hypersensitivity to fluvoxamine maleate.
Potential for Interaction with Monoamine Oxidase Inhibitors
In patients receiving another serotonin reuptake inhibitor drug in combination
with monoamine oxidase inhibitors (MAOI), there have been reports of serious,
sometimes fatal, reactions including hyperthermia, rigidity, myoclonus,
autonomic instability with possible rapid fluctuations of vital signs, and
mental status changes that include extreme agitation progressing to delirium and
coma. These reactions have also been reported in patients who have discontinued
that drug and have been started on a MAOI. Some cases presented with features
resembling neuroleptic malignant syndrome. Therefore, it is recommended that
fluvoxamine maleate not be used in combination with a MAOI, or within 14 days of
discontinuing treatment with a MAOI. After stopping fluvoxamine maleate, at
least 2 weeks should be allowed before starting a MAOI.
BEFORE USING THIS MEDICINE: INFORM YOUR DOCTOR OR
PHARMACIST of all prescription and over-the-counter medicine that you are
taking. This includes astemizole, cyproheptadine, terfenadine, cisapride,
clozapine, fenfluramine, dexfenfluramine, monoamine oxidase inhibitors (MAOIs),
tramadol, or tricyclic antidepressants. Inform your doctor of any other medical
conditions, allergies, pregnancy, or breast-feeding.
Lithium, and possibly tryptophan, may enhance the serotonergic effects of
fluvoxamine; these combinations should therefore be used with caution.
Activation of Mania/Hypomania: During premarketing studies involving
primarily depressed patients, hypomania or mania occurred in approximately 1% of
patients treated with fluvoxamine. Activation of mania/hypomania has also been
reported in a small proportion of patients with major affective disorder who
were treated with other marketed antidepressants. As with all antidepressants,
fluvoxamine maleate should be used cautiously in patients with a history of
mania.
Seizures: During premarketing studies, seizures were reported in 0.2% of
fluvoxamine-treated patients. Fluvoxamine maleate should be used cautiously in
patients with a history of seizures. It should be discontinued in any patient
who develops seizures.
Suicide: The possibility of a suicide attempt is inherent in patients
with depressive symptoms, whether these occur in primary depression or in
association with another primary disorder such as OCD. Close supervision of high
risk patients should accompany initial drug therapy. Prescriptions for
fluvoxamine maleate should be written for the smallest quantity of tablets
consistent with good patient management in order to reduce the risk of overdose.
Use in Patients with Concomitant Illness: Closely monitored clinical
experience with fluvoxamine maleate in patients with concomitant systemic
illness is limited. Caution is advised in administering fluvoxamine maleate to
patients who diseases or conditions that could affect hemodynamic responses or
metabolism.
Interference with Cognitive or Motor Performance: Since any psychoactive
drug may impair judgement, thinking, or motor skills, patients should be
cautioned about operating hazardous machinery, including automobiles, until they
are certain that fluvoxamine maleate therapy does not adversely affect their
ability to engage in such activities.
Drug Interactions
Combined use of fluvoxamine and MAO inhibitors is contraindicated. (See
Warnings)
DO NOT TAKE THIS MEDICINE with terfenadine (Seldane),
astemizole (Hismanal), or cisapride.
In clinical trials, the most commonly observed adverse events associated with
fluvoxamine administration, and not seen at an equivalent incidence among
placebo-treated patients, were gastrointestinal complaints, including nausea
(sometimes accompanied by vomiting), constipation, anorexia, diarrhea and
dyspepsia; CNS complaints, including somnolence, dry mouth, nervousness,
insomnia, dizziness, tremor and agitation; and asthenia. Abnormal (mostly
delayed) ejaculation was frequently reported by patients with obsessive
compulsive disorder, primarily at doses over 150 mg/day.
In a pool of two studies involving only patients with OCD, the following
additional events were identified: dry mouth, decreased libido, urinary
frequency, anorgasmia, rhinitis and taste perversion.
Physical/Psychological Dependence:
The potential for abuse, tolerance and physical dependence with fluvoxamine
maleate has been studied in a nonhuman primate model. No evidence of dependency
phenomena was found.
Generally, it is not possible to predict on the basis of preclinical or
premarketing clinical experience the extent to which a CNS active drug will be
misused, diverted, and/or abused once marketed. Consequently, physicians should
carefully evaluate patients for a history of drug abuse and follow such patients
closely, observing them for signs of fluvoxamine maleate misuse or abuse (i.e.,
development of tolerance, incrementation of dose, drug-seeking behavior).
Signs and Symptoms
Symptoms of overdose may include drowsiness, vomiting, diarrhea, and dizziness.
Cardiac disturbances, liver function disturbances, convulsions and coma have
also been reported.
Of the 354 cases of deliberate or accidental overdose involving fluvoxamine
maleate reported, there were 19 deaths. Of the 19 deaths, 2 were in patients
taking fluvoxamine maleate alone and the remaining 17 were in patients taking
fluvoxamine maleate along with other drugs.
Treatment
If you or someone you know may have used more than the recommended dose of this
medicine, contact your local poison control center or emergency room
immediately.
There are no specific antidotes for fluvoxamine maleate.
An unobstructed airway should be established with maintenance of respiration as
required. Vital signs and ECG should be monitored. Administration of activated
charcoal may be as effective as emesis or lavage and should be considered in
treating overdose. Since absorption with overdose may be delayed, measures to
minimize absorption may be necessary for up to 24 hours post-ingestion.
In managing overdosage, consider the possibility of multiple drug involvement.
Several weeks (up to 8 weeks) may pass before you feel the full effect of this
medicine.
- Follow the directions for using this medicine provided by your doctor.
- Store this medicine at room temperature, away from heat and light.
- Continue to take this medicine even if you feel better.
- If you miss a dose of this medicine and you are taking 1 dose daily,
take the missed dose if you remember the same day. Skip the missed dose if
you do not remember until the next day. If you miss a dose of this medicine
and you are taking more than 1 dose a day, skip the missed dose and go back
to your regular dosing schedule. Do NOT take 2 doses at once.
Additional Information: Do not share this medicine with others for
whom it was not prescribed. Do not use this medicine for other health
conditions. Keep this medicine out of the reach of children.
The recommended starting dose for fluvoxamine maleate is 50 mg, administered
as a single daily dose at bedtime. In the controlled clinical trials
establishing the effectiveness of fluvoxamine maleate in OCD, patients were
titrated within a dose range of 100 to 300 mg/day. Consequently, the dose should
be increased in 50 mg increments every 4 to 7 days, as tolerated, until maximum
therapeutic benefit is achieved, not exceed 300 mg per day. It is advisable that
a total daily dose of more than 100 mg should be given in two divided doses. If
the doses are not equal, the larger dose should be given at bedtime.
Dosage for Elderly or Hepatically Impaired Patients: Elderly patients
and those with hepatic impairment have been observed to have a decreased
clearance of fluvoxamine maleate. Consequently, it may be appropriate to modify
the initial dose and the subsequent dose titration for these patient groups.
Maintenance/Continuation Extended Treatment: Although the efficacy of
fluvoxamine maleate beyond 10 weeks of dosing for OCD has not been documented in
controlled trials, OCD is a chronic condition, and it is reasonable to consider
continuation for a responding patient. Dosage adjustments should be made to
maintain the patient on the lowest effective dosage, and patients should be
periodically reassessed to determine the need for continued treatment.
Tablets:: 50 mg and 100 mg
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Reviewed: 01/2006
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