Truvada Dosing for PrEP
The recommended standard dose of Truvada for HIV Pre-Exposure Prophylaxis (PrEP) is one tablet (containing emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg) taken orally once daily, regardless of food intake. 1, 2
Dosing Regimens Based on Risk Group
For All Populations at Risk:
For Men who have Sex with Men (MSM):
Option 1 - Daily dosing with accelerated start:
Option 2 - 2-1-1 (on-demand) dosing (for MSM only):
For Other Risk Groups (heterosexual men and women, people who inject drugs):
- Daily dosing only (on-demand dosing not recommended)
- Protection achieved approximately 7 days after initiation
- Continue for 7 days after last risk exposure 1
Special Populations
Renal Impairment:
- Not recommended for patients with creatinine clearance <60 mL/min 2
- For MSM with creatinine clearance between 30-60 mL/min who have osteopenia/osteoporosis:
Pregnancy and Breastfeeding:
- Daily Truvada is recommended for at-risk pregnant individuals 1
- Safety data for pregnancy is incomplete, but no harm has been reported 2
Required Testing Before Initiation
- Combined HIV antibody and antigen testing (HIV RNA if acute infection suspected)
- Serum creatinine level
- Hepatitis B surface antigen
- Hepatitis C antibody (if not known to be previously positive)
- STI screening (gonorrhea and chlamydia at all potential exposure sites) 1, 2
Monitoring During PrEP
- At 1 month: HIV antibody/antigen test
- Quarterly:
- HIV antibody/antigen test
- STI screening
- Pregnancy testing (if applicable)
- Every 6 months:
Important Clinical Considerations
- Adherence is critical for PrEP efficacy - effectiveness exceeds 90% with good adherence 3
- The risk of developing resistance is low (<0.1%) when PrEP is properly prescribed 3
- Truvada does not protect against other STIs, so regular STI screening is essential 1, 2
- Efficacy varies by risk group and adherence levels, with demonstrated risk reductions of 44-75% in major clinical trials 4
Pitfalls to Avoid
- Starting PrEP without confirming HIV-negative status can lead to resistance development
- Inadequate renal monitoring in patients with or at risk for kidney dysfunction
- Using on-demand dosing in populations other than MSM, where this approach has not been validated
- Failing to continue PrEP for the appropriate duration after last exposure (2 days for MSM, 7 days for others) 1, 2