Zyven OD (Pristiq / Desvenlafaxine)100 Mg – 100 tablet

Zyven OD (Pristiq / Desvenlafaxine)100 Mg – 100 tablet

$103.53

Each Zyven OD Tablet contains 100 mg Desvenlafaxine with 100 tablets a box used in the treatment of major depressive disorders.

ATC Classification: N06AX23
Active Ingrediant: Desvenlafaxine
Generic Name: Zyven OD
Manufacturer: Zydus
Strength: 100 Mg
Dosage Type: Tablet
Packaging Type: Blister in Box
Contains: 100 Tabs

Description

 

Pronunciation

(des ven la FAX een)

 

Medication Safety Issues

Sound-alike/look-alike issues:

Pristiq may be confused with PriLOSEC

Geriatric Patients: High-Risk Medication:

Beers Criteria: Serotonin/Norepinephrine Reuptake Inhibitors (SNRIs) are identified in the Beers Criteria as potentially inappropriate medications to be used with caution in patients 65 years and older due to its potential to cause or exacerbate syndrome of inappropriate antidiuretic hormone secretion (SIADH) or hyponatremia; monitor sodium concentration closely when initiating or adjusting the dose in older adults (Beers Criteria [AGS 2019]).

 

Storage/Stability

Store at 20°C to 25°C (68°F to 77°F); excursions permitted to 15°C to 30°C (59°F to 86°F).

 

Adverse Reactions

>10%:

Central nervous system: Dizziness (10% to 13%), insomnia (9% to 12%)

Dermatologic: Hyperhidrosis (10% to 11%)

Gastrointestinal: Nausea (22% to 26%), xerostomia (11% to 17%)

1% to 10%:

Cardiovascular: Orthostatic hypotension (elderly 8%), syncope (<2%), tachycardia (<2%), hypertension (dose related; ≤1% of patients taking 50 to 100 mg daily had sustained diastolic BP ≥90 mm Hg)

Central nervous system: Drowsiness (≤9%), fatigue (7%), anxiety (3% to 5%), delayed ejaculation (1% to 5%), abnormal dreams (2% to 3%), anorgasmia (males ≤3%; females 1%), jitteriness (2%), vertigo (≤2%), depersonalization (<2%), dystonia (<2%), seizure (<2%), disturbance in attention (1%), yawning (1%), male sexual disorder (≤1%)

Dermatologic: Alopecia (<2%), skin photosensitivity (<2%), skin rash (<2%)

Endocrine & metabolic: Decreased libido (males 4% to 5%), increased serum cholesterol (increased by ≥50 mg/dL and ≥261 mg/dL: 3% to 4%), increased serum prolactin (<2%), weight gain (<2%), hot flash (1%), increased LDL cholesterol (increased by ≥50 mg/dL and ≥190 mg/dL: ≤1%)

Gastrointestinal: Constipation (9%), decreased appetite (5% to 8%), vomiting (≤4%), bruxism (<2%)

Genitourinary: Proteinuria (5% to 8%), erectile dysfunction (3% to 6%), urinary retention (<2%), ejaculation failure (≤1%), urinary hesitancy (≤1%)

Hepatic: Abnormal hepatic function tests (<2%)

Hypersensitivity: Angioedema (<2%)

Neuromuscular & skeletal: Tremor (≤3%), stiffness (<2%), weakness (<2%)

Ophthalmic: Blurred vision (3% to 4%), mydriasis (2%)

Otic: Tinnitus (≤2%)

Frequency not defined: Cardiovascular: Coronary occlusion, ischemic heart disease, myocardial infarction

<1%, postmarketing, and/or case reports: Acute pancreatitis, angle-closure glaucoma, cardiomyopathy (takotsubo), Stevens-Johnson syndrome

Brand

Zydus

Additional information

Active Ingrediant

Generic Name

Alternate Names

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Strength

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