Apretude Generic Name & Formulations
Legal Class
General Description
Pharmacological Class
How Supplied
Manufacturer
Generic Availability
Mechanism of Action
Apretude Indications
Indications
Apretude Dosage and Administration
Adult
Children
Apretude Contraindications
Contraindications
Apretude Boxed Warnings
Boxed Warning
Apretude Warnings/Precautions
Warnings/Precautions
Provide comprehensive management to reduce the risk of HIV-1 acquisition. Counsel individuals on the use of other prevention measures (eg, condom use, knowledge of partner(s)’ HIV-1 status, regular testing for STIs). Potential risk of resistance: reassess for HIV-1 acquisition risk; test before each inj to confirm HIV-1 negative status. Discontinue immediately if hypersensitivity reactions occur. Monitor liver function; discontinue if hepatotoxicity is suspected. Promptly evaluate if depressive symptoms occur. Long-acting properties: residual drug concentrations may remain ≥12months. Severe hepatic impairment. Severe renal impairment or ESRD: monitor. Elderly. Pregnancy: potential for fetal exposure. Nursing mothers: assess benefit/risk to infant (not recommended if acute HIV-1 infection is suspected).
Apretude Pharmacokinetics
Absorption
Median time to reach maximum concentration: 7 days.
Distribution
Plasma protein bound: >99.8%. Blood-to-plasma ratio: 0.52. CSF-to-plasma concentration ratio (median [range]): 0.003 (0.002–0.004).
Elimination
Apretude Interactions
Interactions
See Contraindications. Antagonized by strong UGT1A1 or 1A9 inducers. Antagonized by rifabutin (see Adult dose).
Apretude Adverse Reactions
Adverse Reactions
Apretude Clinical Trials
See Literature
Apretude Note
Not Applicable
Apretude Patient Counseling
See Literature
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