FOSAMPRENAVIR CALCIUM
  • FOSAMPRENAVIR CALCIUM (Generic for LEXIVA)

  • QTY 60 • 700 MG • Tablet • Near 77381

FOSAMPRENAVIR /Lexiva(FOS am pren a veer) is an antiretroviral medicine. It is used with other medicines to treat HIV. This medicine is not a cure for HIV. This medicine can lower, but not fully prevent, the risk of spreading HIV to others.

FOSAMPRENAVIR CALCIUM (Generic for LEXIVA) Lifestyle Interactions

Fosamprenavir Calcium 700mg, Oral tablet

Grapefruit juice

· Severity: Mild

· Notes for Consumers: Although an interaction is possible, it is usually okay to drink grapefruit juice or eat grapefruits while taking Fosamprenavir. In theory, side effects from Fosamprenavir such as diarrhea, headache, or rash might get worse if you drink grapefruit juice or eat grapefruits, but significant interactions have not been reported. Do not greatly alter your normal grapefruit and grapefruit juice intake while taking Fosamprenavir.

· Notes for Professionals: Fosamprenavir is a substrate of the CYP3A4 isoenzyme and theoretically the drug's metabolism may be inhibited by grapefruit juice, resulting in an increase in fosamprenavir plasma concentrations. The extent and clinical significance of this interaction are unknown. Advise patients not to significantly alter their grapefruit or grapefruit juice intake while taking fosamprenavir.

Fosamprenavir Calcium 700mg, Oral tablet

Marijuana

· Severity: Moderate

· Notes for Consumers: The effects of marijuana may be increased and side effects may get worse if it is combined with this medicine. Do not drive or operate machinery until you know how this combination will affect you. Contact your health care provider right away if you notice slurred speech, confusion, severe drowsiness, increased heart rate, or any other new or unusual side effects.

· Notes for Professionals: The pharmacokinetic parameters of anti-retroviral medications (anti-retroviral non-nucleoside reverse transcriptase inhibitors (NNRTIs), anti-retroviral nucleoside reverse transcriptase inhibitors (NRTIs), anti-retroviral nucleotide reverse transcriptase inhibitors, and anti-retroviral protease inhibitors) metabolized through the CYP isoenzyme system are slightly altered by smoked and oral marijuana. Despite this interaction, marijuana is not expected to adversely affect anti-retroviral efficacy. However, the incidence of marijuana associated adverse effects may change following coadministration with anti-retroviral drugs. Many anti-retrovirals are inhibitors of CYP3A4, an isoenzyme partially responsible for the metabolism of marijuana's most psychoactive compound, delta-9-tetrahydrocannabinol (Delta-9-THC). When given concurrently with anti-retrovirals, the amount of Delta-9-THC converted to the active metabolite 11-hydroxy-delta-9-tetrahydrocannabinol (11-OH-THC) may be reduced. These changes in Delta-9-THC and 11-OH-THC plasma concentrations may result in an altered marijuana adverse event profile.

<b>DISCLAIMER:</b><em> This drug information content is provided for informational purposes only and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Patients should always consult their physician with any questions regarding a medical condition and to obtain medical advice and treatment. Drug information is sourced from GSDD (Gold Standard Drug Database ) provided by Elsevier.</em>

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