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Frequently bought together
EFEXOR XR 150MG 14CAP
- Sku : I-001861
Key features
Efexor XR 150 mg is a prolonged-release capsule containing venlafaxine hydrochloride 150 mg. It belongs to the SNRI antidepressant class and works by helping to balance serotonin and norepinephrine levels in the brain. It is used for the treatment of major depressive disorder and certain anxiety-related conditions. It is supplied as a pack of 14 prolonged-release capsules.- Brand: EFEXOR
- Active Ingredient: VENLAFAXINE HYDROCHLORIDE 150mg
- Strength: 150mg
- Dosage Form: Prolonged-release capsule
- Pack Size: 14 Capsules
- Route: Oral use
- Prescription Status: Prescription
- Therapeutic Class: Psychiatric
- Pharmacological Group: Other Antidepressants
- Drug Class: SNRI Antidepressant (Serotonin-Norepinephrine Reuptake Inhibitor)
- Manufacturer: PFIZER
- Country of Origin: Ireland
- SFDA Registration No.: 10-5825-23
- Shelf Life: 36 months
- Storage: do not store above 25°c
- Psych Class: Antidepressant-SNRI
- Controlled Substance: No
Frequently bought together
Indications
Off-Label Uses
Commonly used off-label for neuropathic pain (including diabetic neuropathy), migraine prophylaxis, menopausal hot flashes/vasomotor symptoms, and PTSD (evidence varies).
Dosage & Administration
Initial Dose
75mg once daily (37.5mg once daily for panic disorder)
Maintenance Dose
75mg to 225mg once daily.
Maximum Dose
225mg per day for most indications.
Children's Dosage
Not approved for children or adolescents under 18 years
Dose Adjustment Notes
Titrate gradually based on response/tolerability (commonly in 75 mg increments at intervals of at least several days); reduce total daily dose in renal impairment and in hepatic impairment (often ~50% reduction), and taper gradually when discontinuing to minimize withdrawal symptoms.
Safety & Warnings
Contraindications
Hypersensitivity to venlafaxine/desvenlafaxine or any excipients; concomitant use with MAOIs or within 14 days of stopping an MAOI (and allow at least 7 days after stopping venlafaxine before starting an MAOI).
Warnings & Precautions
Monitor for clinical worsening/suicidality (especially in patients <25) during initiation and dose changes; risk of serotonin syndrome with serotonergic agents/MAOI-type drugs; monitor blood pressure (dose-related increases); use caution in seizure disorders and bipolar disorder (mania/hypomania); risk of hyponatremia/SIADH (higher in elderly/diuretics); increased bleeding risk with antiplatelets/NSAIDs/anticoagulants; taper gradually to avoid discontinuation syndrome; mydriasis/angle-closure glaucoma risk-use caution in patients with raised intraocular pressure/narrow angles; consider cardiac risk/ECG monitoring in overdose or high-risk patients.
Age Restriction
Not approved under 18 years.
Drug Interactions
Interaction Severity
MAJOR/contraindicated: MAOIs (including linezolid and IV methylene blue) due to serotonin syndrome risk. MODERATE: other serotonergic agents (SSRIs/SNRIs, triptans, tramadol, lithium, St John’s wort) due to serotonin syndrome; anticoagulants/antiplatelets/NSAIDs due to bleeding risk; strong CYP2D6 inhibitors may alter venlafaxine/ODV exposure (clinical significance varies).
Food Interaction
Take with food.
Special Populations
Pregnancy
Caution
Children
Not approved for children or adolescents under 18 years
Elderly
No specific dose adjustment required based on age alone; however, start at lower doses and titrate cautiously. Monitor blood pressure and serum sodium closely due to increased risk of hyponatremia and falls
Liver Impairment
Mild-to-moderate hepatic impairment (Child-Pugh A-B): reduce total daily dose by ~50%. Severe hepatic impairment/cirrhosis (Child-Pugh C): reduce by ≥50% (often more) and titrate cautiously.
Storage & Patient Advice
Patient Counseling
Take once daily with food; swallow XR capsule whole (do not crush/chew/open). Do not stop abruptly-taper with prescriber to avoid withdrawal. Expect benefit to build over several weeks. Avoid alcohol and use caution with driving until effects are known. Monitor/report elevated blood pressure, worsening mood/suicidal thoughts, and symptoms of serotonin syndrome (agitation, confusion, sweating, tremor, fast heartbeat). Tell clinicians about all medicines/herbals (e.g., St John’s wort, triptans, tramadol, NSAIDs/anticoagulants).
Monitoring Requirements
Monitor blood pressure (baseline and periodically) and heart rate; monitor for clinical worsening/suicidality especially early and after dose changes; monitor for serotonin syndrome when combined with serotonergic drugs; consider serum sodium in at-risk patients (e.g., elderly/diuretics) and weight.
Pharmacology
Duration of Effect
Antidepressant/anxiolytic clinical effect is sustained with continued daily dosing; each extended-release dose provides ~24-hour coverage.
Half-Life
Venlafaxine (parent drug): ~5 hours. O-desmethylvenlafaxine (active metabolite): ~11 hours.
Bioavailability
Approximately 45% (venlafaxine); XR provides slower absorption with similar overall bioavailability compared with immediate-release.
Metabolism
Extensive hepatic metabolism primarily via CYP2D6 to active O-desmethylvenlafaxine (ODV), with minor contribution from CYP3A4 and other pathways.
Protein Binding
Low protein binding: venlafaxine ~27% and ODV ~30%.
Product Information
OTC Alternatives
No OTC alternative
Psych Class
Antidepressant-SNRI
Controlled Substance
No
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