Drug Comparison

For educational purposes only — a decision-support tool, not a substitute for clinical judgment.

Side-by-side rubric across 96 psychiatric medications. Every rating traces to a verbatim primary-source quote — click any cell to see it.

How to read this tool
Rating scale
Favorable / lower than class baseline
± Minimal / equivocal
+ Low / uncommon
++ Moderate / common
+++ High / very common
++++ Very high / class-outlier
Frequency vs severity
F = frequency, S = severity. Each gets its own pill colored on the same traffic-light scale: greenblueyelloworangered. Click any cell for incidence percentages and NNH.
Evidence tier
A Network meta-analysis / RCT / FDA label
B Cohort / registry / pooled label data
C Expert review / textbook / case series
Sourcing
Click any cell to see the verbatim source quote and citation. Missing data shows n/a.
Data depth
++ Graded — frequency + severity, primary-source traces
+ FDA label — §6 frequency only (dashed border). Click for sub-types.
  Blank — not yet checked (not “absent”)
±++++++++++ABCF = frequency · S = severity · Dashed border = FDA label only · Click cell for details
1 drug selected — Venlafaxine(click to collapse)
1/4 selected
Venlafaxine
Effexor
Serotonin-Norepinephrine Reuptake Inhibitor
FDA-approved indications
  • Major depressive disorder (adults)
  • Generalized anxiety disorder (adults)
  • Social anxiety disorder (adults)
  • Panic disorder, with or without agoraphobia (adults)
Off-label uses
  • Social anxiety disorder
  • Panic disorder
  • PTSD
Half-life5 hours (ODV active metabolite: 11 hours)
Next:Taper Venlafaxine
Decision GuideWhen to pick each / when to consider an alternative
Venlafaxine
Consider when
  • Treatment-resistant depression or SSRI non-response — top-tier efficacy in Cipriani 2018 NMA; ~6% remission advantage over SSRIs
  • Depression with comorbid anxiety disorders — FDA-approved for GAD, SAD, and panic disorder alongside MDD
  • Ascending dose-response needed — dose-dependent NE engagement above 150 mg allows titration from SSRI-like to full SNRI effect
  • Pain comorbidity with depression — noradrenergic effects at higher doses assist with pain; though duloxetine has FDA pain indications
  • +1 more
Consider an alternative when
  • Adherence may falter — worst discontinuation syndrome among SNRIs (incidence 0.40, Henssler 2024); withdrawal within 24–48 h of missed dose
  • Sexual dysfunction is a concern — total SD OR 24.82 (Serretti 2009); highest SD risk among commonly prescribed antidepressants in Danish cohort
  • Uncontrolled or borderline hypertension — dose-dependent BP elevation especially >150 mg; most pronounced BP effect among SNRIs
  • Overdose risk present — cardiotoxicity in overdose; UK regulatory CI for heart disease; higher toxicity index than SSRIs
  • +1 more
Axis
Venlafaxine
SNRI
Boxed Warnings
Suicidality (boxed warning)
CNS
Sedation / somnolence
Activation / insomnia
Emotional blunting
Seizure risk
Metabolic
Weight gain
Metabolic (glucose / lipids)
Autonomic
Anticholinergic burden
Orthostatic hypotension
Sweating
Angle-closure glaucoma
Cardiac
QTc prolongation
Blood pressure elevation
Heart rate / tachycardia
GI
Nausea / GI (general)
Hepatic
Liver enzymes / hepatotoxicity
Electrolytes
Hyponatremia / SIADH
Sexual
Sexual dysfunction
Discontinuation
Withdrawal / discontinuation
Interactions
Serotonin syndrome risk
CYP interactions / DDI profile
Safety
Bleeding risk
Overdose toxicity
Pregnancy
Teratogenicity
Lactation / breastfeeding safety

Safety: Every rating traces to a verbatim primary-source quote. Click any cell to audit. Stubs are disabled until calibrated. This tool surfaces published evidence — it does not replace clinical judgment.