Medication Dosing Guidelines for Post-Traumatic Stress Disorder (PTSD)
Prazosin is the first-line pharmacological treatment for PTSD-associated nightmares, with sertraline and paroxetine recommended as first-line treatments for overall PTSD symptoms. 1
First-Line Pharmacological Treatments
SSRIs (First-line for overall PTSD symptoms)
Sertraline (Zoloft)
- Initial dose: 25 mg/day for first week
- Therapeutic range: 50-200 mg/day
- Mean effective dose in clinical trials: 146-151 mg/day
- Administered as a single daily dose with or without food 2
Paroxetine (Paxil)
- Initial dose: 20 mg/day
- Therapeutic range: 20-50 mg/day
- Dose changes should occur in 10 mg/day increments at intervals of at least 1 week
- Maximum dose: 50 mg/day
- Administered as a single daily dose with or without food, usually in the morning 3
Alpha-1 Adrenergic Antagonist (First-line for PTSD-associated nightmares)
- Prazosin
- Initial dose: 1 mg at bedtime
- Increase by 1-2 mg every few days until effective dose is reached
- Average effective dose: 3 mg (range 1-15 mg)
- Higher doses (9.5-15.6 mg/day) may be needed for combat-related PTSD
- Monitor for orthostatic hypotension 1
- Note: Recent evidence has led to downgrading the recommendation strength, but prazosin remains the first choice for PTSD-related nightmares 1
Second-Line Pharmacological Treatments
For PTSD-Associated Nightmares
Clonidine
- Dose range: 0.2-0.6 mg in divided doses
- Monitor for hypotension
- Level C recommendation (lower evidence than prazosin) 1
Trazodone
- Dose range: 25-600 mg (mean effective dose: 212 mg)
- Common side effects: daytime sedation, dizziness, headache, priapism, orthostatic hypotension
- Level C recommendation 1
Other Second-Line Options for PTSD Symptoms
Venlafaxine
- Dose range: 32.5-300 mg/day
- Note: Limited efficacy for nightmares specifically 1
Fluoxetine
- Dose range: 20-60 mg/day
- Similar efficacy to other SSRIs 4
Escitalopram
- Initial dose: 10 mg daily for 4 weeks
- May increase to 20 mg daily thereafter 5
Third-Line and Adjunctive Treatments
Topiramate
- Initial dose: 25 mg/day
- Titrate up to effect or maximum 400 mg/day
- Median effective dose: 150 mg/day 1
Atypical Antipsychotics (as augmentation)
- Consider for patients with partial response to SSRIs
- Risperidone has the strongest evidence as an add-on therapy 6
Low-dose Cortisol
- Dose: 10 mg/day (either in morning or half at noon and half in evening)
- Limited evidence but may reduce nightmare frequency 1
Gabapentin
- Dose range: 685-1344 mg/day
- Higher doses (mean 1344 mg) associated with better response 1
Fluvoxamine
- Dose range: 50-300 mg/day
- Limited evidence but may reduce combat-related nightmares 1
Medications to Avoid in PTSD
Benzodiazepines
Cannabis and cannabis-derived products
- Not recommended due to insufficient evidence of efficacy and potential harms 1
Special Considerations
Elderly or Debilitated Patients
- Start with lower doses (e.g., paroxetine 10 mg/day)
- Increase doses more gradually
- Maximum dose should not exceed 40 mg/day 3
Pregnancy (Third Trimester)
- Consider tapering SSRIs during third trimester due to potential neonatal complications
- Carefully weigh risks and benefits 3
Combination Treatment
- Consider combining psychotherapy (particularly trauma-focused CBT) with medication for optimal outcomes 1
Monitoring and Duration of Treatment
- Assess response using standardized symptom rating scales 1
- Continue effective treatment for at least 6-12 months to decrease relapse rates 4
- Periodically reassess to determine need for continued treatment 2, 3
- Monitor for side effects, particularly orthostatic hypotension with prazosin and clonidine 1
Common Pitfalls and Caveats
- Antidepressant efficacy may be reduced when combined with prazosin (particularly in combat veterans) 1
- SSRIs may initially worsen anxiety symptoms; consider starting with subtherapeutic "test" dose 1
- Discontinuation syndrome can occur with abrupt cessation of shorter-acting SSRIs (particularly paroxetine) 1
- Response rates to SSRIs rarely exceed 60%, with full remission in only 20-30% of patients 6
- Nefazodone is not recommended as first-line therapy due to increased risk of hepatotoxicity 1