Classes
DEA Class; Rx
Common Brand Names; Luvox, Luvox CR (DSC)
- Antidepressants, SSRIs
Description
Selective serotonin reuptake inhibitor; little or no affinity for dopamine, alpha-adrenergic histamine, or cholinergic receptor
Indications
Indicated for Obsessive-Compulsive Disorder, Social Phobia (Off-label), Panic Disorder (Off-label), Posttraumatic Stress Disorder (Off-label)
Contraindications
Hypersensitivity
Adverse Effects
- Nausea (40%)
- Headache (22-35%)
- Somnolence (22-27%)
- Weakness (14-26%)
- Insomnia (20-35%)
- Diarrhea (11-18%)
- Dizziness (11-15%)
- Xerostomia (10-14%)
- Anorexia (6-14%)
- Abnormal ejaculation (8-11%)
- Pain (10%)
- Dyspepsia (8-10%)
- Constipation (4-10%)
- Decreased libido (2-10%)
- Upper respiratory infections (9%)
- Anxiety (5-8%)
- Tremor (5-8%)
- Sweating (6-7%)
- Vomiting (4-6%)
- Abdominal pain (5%)
- Myalgia (5%)
- Abnormal taste (2-5%)
- Bruising (4%)
- Abnormal dreams (3%)
- Abnormal thinking (3%)
- Chest pain (3%)
- Palpitation (3%)
- Agitation (2-3%)
- Vasodilation (2-3%)
- Hypertension (1-2%)
- Increased LFTs (1-2%)
- Weight change (1-2%)
- Manic reaction
- <1%
- Activation of mania/hypomania, seizures (discontinue)
- Sinusitis
- Edema
- Amnesia
- Apathy
- Asthenia
- Malaise
- Nervousness
- Dry mouth
- Myoclonus
- Cough
Warnings
Conflicting evidence regarding use of SSRIs during pregnancy and increased risk of persistent pulmonary hypertension of the newborn (see Pregnancy)
In neonates exposed to SNRIs/SSRIs late in third trimester: Risk of complications such as feeding difficulties, irritability, and respiratory problems
Risk of mydriasis; may trigger angle closure attack in patients with angle closure glaucoma with anatomically narrow angles without a patent iridectomy
May need to modify dose for hepatic impairment; titrate at smaller increments and longer intervals
Clinical worsening and suicide ideation may occur despite medication in adolescents and young adults (18-24 years); prescriptions should be written for the smallest quantity consistent with good patient care
May worsen mania symptoms or precipitate mania in patients with bipolar disorder
May impair platelet aggregation; increases risk of bleeding in patients taking anticoagulants/antiplatelets concomitantly
Do not use concurrently with alosetron, astemizole, cisapride, pimozide, terfenadine, or tizanidine due to QT prolongation risk
Potentially life-threatening serotonin syndrome has been reported with drugs that impair serotonin metabolism (in particular, MAOIs, including nonpsychiatric MAOIs, such as linezolid and IV methylene blue); it has also been reported with reported with SNRIs and SSRIs, including fluvoxamine, alone but particularly with concomitant use of serotonergic drugs (including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, amphetamines, and St. John’s Wort (see Contraindications)
May impair ability to operate heavy machinery and other tasks requiring mental alertness
Bone fractures have been associated with antidepressant treatment; consider possibility of fragility fracture if patient presents with pain, joint tenderness, or swelling
Impaired glucose control (hyperglycemia or hypoglycemia) reported; monitor for signs/symptoms of loss of glucose control, especially in patients with diabetes
Pregnancy and Lactation
There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to antidepressants during pregnancy
Data from published literature report presence of drug in human milk; no adverse effects on breastfed infant have been reported in most cases of maternal use of fluvoxamine during breastfeeding
Maximum Dosage
Obsessive-Compulsive Disorder
Conventional tablets
50 mg qHS initially; may increase by 50 mg/day q4-7Days up to 100-300 mg/day
Dose >100 mg/day should be divided q12hr
Social Phobia (Off-label)
Immediate release
50 mg PO qDay; may increase by 50 mg at 1 week interval; usual dose range is 100-300 mg/day
Panic Disorder (Off-label)
25-50 mg PO qDay; after several days, gradually increase to 100-200 mg/day; may increase to 300 mg/day for patients who fail to respond after several weeks of treatment
Pediatric
Obsessive-Compulsive Disorder
<8 years: Safety and efficacy not established
Ages 8-17 years (conventional tablets): 25 mg PO qHS initially; may titrate by 25 mg/day increments every 4-7 days to 50-200 mg/day
Not to exceed 200 mg (for ages 8-11 years) or 300 mg for adolescents
Give doses >50 mg/day divided q12hr
Geriatic
The elderly are prone to SSRI/SNRI-induced hyponatremia; monitor closely
How supplied
Fluvoxamine maleate
tablets
- 25mg
- 50mg
- 100mg