FDA label d93799ad-308b-4f54-b8d5-07402cd8882e
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- SPL set ID
- 9b370904-d2cd-4585-bc48-a8110621c8bd
- SPL ID
- d93799ad-308b-4f54-b8d5-07402cd8882e
- Version
- 1
- Effective date
- 2010-04-13
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:03:03
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| spl id | d93799ad-308b-4f54-b8d5-07402cd8882e | id | |
| spl set id | 9b370904-d2cd-4585-bc48-a8110621c8bd | set_id |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS ALERT: Find out about medicines that should not be taken with VIRACEPT . This statement is included on the product's bottle label. Drug Interactions (also see PRECAUTIONS ) Nelfinavir is an inhibitor of the CYP3A enzyme. Coadministration of VIRACEPT and drugs primarily metabolized by CYP3A may result in increased plasma concentrations of the other drug that could increase or prolong its therapeutic and adverse effects. Caution should be exercised when inhibitors of CYP3A, including VIRACEPT, are coadministered with drugs that are metabolized by CYP3A and that prolong the QT interval. (See ADVERSE REACTIONS: Post-Marketing Experience .) Nelfinavir is metabolized by CYP3A and CYP2C19. Coadministration of VIRACEPT and drugs that induce CYP3A or CYP2C19 may decrease nelfinavir plasma concentrations and reduce its therapeutic effect. Coadministration of VIRACEPT and drugs that inhibit CYP3A or CYP2C19 may increase nelfinavir plasma concentrations. (Also see PRECAUTIONS: Table 10: Drugs That Should Not Be Coadministered With VIRACEPT , Table 11: Established and Other Potentially Significant Drug Interactions . ) Concomitant use of VIRACEPT with lovastatin or simvastatin is not recommended. Caution should be exercised if HIV protease inhibitors, including VIRACEPT, are used concurrently with other HMG-CoA reductase inhibitors that are also metabolized by the CYP3A pathway (e.g., atorvastatin). (Also see Tables 6 and 7: Drug Interactions ). The risk of myopathy including rhabdomyolysis may be increased when protease inhibitors, including VIRACEPT, are used in combination with these drugs. Particular caution should be used when prescribing sildenafil, or other PDE5 inhibitors, in patients receiving protease inhibitors, including VIRACEPT. Coadministration of these drugs is expected to substantially increase PDE5 inhibitor concentrations and may result in an increase in PDE5 inhibitor-associated adverse events, including hypotension, visual changes, and priapism. (See PRECAUTIONS, Drug Interactions and Information for Patients , and the complete prescribing information for sildenafil and other PDE5 inhibitors.) Concomitant use of St. John's wort (hypericum perforatum) or St. John's wort containing products and VIRACEPT is not recommended. Coadministration of St. John's wort with protease inhibitors, including VIRACEPT, is expected to substantially decrease protease inhibitor concentrations and may result in sub-optimal levels of VIRACEPT and lead to loss of virologic response and possible resistance to VIRACEPT or to the class of protease inhibitors. Patients with Phenylketonuria Patients with Phenylketonuria: VIRACEPT Oral Powder contains 11.2 mg phenylalanine per gram of powder. Diabetes mellitus/Hyperglycemia New onset diabetes mellitus, exacerbation of pre-existing diabetes mellitus and hyperglycemia have been reported during post-marketing surveillance in HIV-infected patients receiving protease inhibitor therapy. Some patients required either initiation or dose adjustments of insulin or oral hypoglycemic agents for treatment of these events. In some cases diabetic ketoacidosis has occurred. In those patients who discontinued protease inhibitor therapy, hyperglycemia persisted in some cases. Because these events have been reported voluntarily during clinical practice, estimates of frequency cannot be made and a causal relationship between protease inhibitor therapy and these events has not been established.
Adverse reactions cross-check#
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adverse reactions
ADVERSE REACTIONS The safety of VIRACEPT was studied in over 5000 patients who received drug either alone or in combination with nucleoside analogues. The majority of adverse events were of mild intensity. The most frequently reported adverse event among patients receiving VIRACEPT was diarrhea, which was generally of mild to moderate intensity. Drug-related clinical adverse experiences of moderate or severe intensity in ≥ 2% of patients treated with VIRACEPT coadministered with d4T and 3TC (Study 542) for up to 48 weeks or with ZDV plus 3TC (Study 511) for up to 24 weeks are presented in Table 12. Table 12 Percentage of Patients with Treatment-Emergent Includes those adverse events at least possibly related to study drug or of unknown relationship and excludes concurrent HIV conditions Adverse Events of Moderate or Severe Intensity Reported in ≥ 2% of Patients Study 511 24 weeks Study 542 48 weeks Adverse Events Placebo + ZDV/3TC (n=101) 500 mg TID VIRACEPT + ZDV/3TC (n=97) 750 mg TID VIRACEPT + ZDV/3TC (n=100) 1250 mg BID VIRACEPT + d4T/3TC (n=344) 750 mg TID VIRACEPT + d4T/3TC (n=210) Digestive System Diarrhea 3% 14% 20% 20% 15% Nausea 4% 3% 7% 3% 3% Flatulence 0 5% 2% 1% 1% Skin/Appendages Rash 1% 1% 3% 2% 1% Adverse events occurring in less than 2% of patients receiving VIRACEPT in all phase II/III clinical trials and considered at least possibly related or of unknown relationship to treatment and of at least moderate severity are listed below. Body as a Whole : abdominal pain, accidental injury, allergic reaction, asthenia, back pain, fever, headache, malaise, pain, and redistribution/accumulation of body fat (see PRECAUTIONS, Fat Redistribution ). Digestive System : anorexia, dyspepsia, epigastric pain, gastrointestinal bleeding, hepatitis, mouth ulceration, pancreatitis and vomiting. Hemic/Lymphatic System : anemia, leukopenia and thrombocytopenia. Metabolic/Nutritional System : increases in alkaline phosphatase, amylase, creatine phosphokinase, lactic dehydrogenase, SGOT, SGPT and gamma glutamyl transpeptidase; hyperlipemia, hyperuricemia, hyperglycemia, hypoglycemia, dehydration, and liver function tests abnormal. Musculoskeletal System : arthralgia, arthritis, cramps, myalgia, myasthenia and myopathy. Nervous System : anxiety, depression, dizziness, emotional lability, hyperkinesia, insomnia, migraine, paresthesia, seizures, sleep disorder, somnolence and suicide ideation. Respiratory System : dyspnea, pharyngitis, rhinitis, and sinusitis. Skin/Appendages : dermatitis, folliculitis, fungal dermatitis, maculopapular rash, pruritus, sweating, and urticaria. Special Senses : acute iritis and eye disorder. Urogenital System : kidney calculus, sexual dysfunction and urine abnormality. Post-Marketing Experience The following additional adverse experiences have been reported from postmarketing surveillance as at least possibly related or of unknown relationship to VIRACEPT: Body as a Whole: hypersensitivity reactions (including bronchospasm, moderate to severe rash, fever and edema). Cardiovascular System: QTc prolongation, torsades de pointes. Digestive System : jaundice. Metabolic/Nutritional System: bilirubinemia, metabolic acidosis. Laboratory Abnormalities The percentage of patients with marked laboratory abnormalities in Studies 542 and 511 are presented in Table 13. Marked laboratory abnormalities are defined as a Grade 3 or 4 abnormality in a patient with a normal baseline value or a Grade 4 abnormality in a patient with a Grade 1 abnormality at baseline. Table 13 Percentage of Patients by Treatment Group With Marked Laboratory Abnormalities Marked laboratory abnormalities are defined as a shift from Grade 0 at baseline to at least Grade 3 or from Grade 1 to Grade 4 in > 2% of Patients Study 511 Study 542 Placebo + ZDV/3TC (n=101) 500 mg TID VIRACEPT + ZDV/3TC (n=97) 750 mg TID VIRACEPT + ZDV/3TC (n=100) 1250 mg BID VIRACEPT + d4T/3TC (n=344) 750 mg TID VIRACEPT + d4T/3TC (n=210) Hematology Hemoglobin 6% 3% 2% 0 0 Neutrophils 4% 3% 5% 2% 1% Lymphocytes 1% 6% 1% 1% 0 Chemistry ALT (SGPT) 6% 1% 1% 2% 1% AST (SGOT) 4% 1% 0 2% 1% Creatine Kinase 7% 2% 2% NA NA Pediatric Population VIRACEPT has been studied in approximately 400 pediatric patients in clinical trials from birth to 13 years of age. The adverse event profile seen during pediatric clinical trials was similar to that for adults. The most commonly reported drug-related, treatment-emergent adverse events reported in the pediatric studies included: diarrhea, leukopenia/neutropenia, rash, anorexia and abdominal pain. Diarrhea, regardless of assigned relationship to study drug, was reported in 39% to 47% of pediatric patients receiving VIRACEPT in 2 of the larger treatment trials. Leukopenia/neutropenia was the laboratory abnormality most commonly reported as a significant event across the pediatric studies.
adverse reactions table
<table width="100%"> <caption>Table 12 Percentage of Patients with Treatment-Emergent<footnote>Includes those adverse events at least possibly related to study drug or of unknown relationship and excludes concurrent HIV conditions</footnote> Adverse Events of Moderate or Severe Intensity Reported in ≥ 2% of Patients</caption> <col align="left" valign="top" width="17%"/> <col align="center" valign="top" width="16%"/> <col align="center" valign="top" width="17%"/> <col align="center" valign="top" width="16%"/> <col align="center" valign="top" width="17%"/> <col align="center" valign="top" width="17%"/> <thead> <tr> <th styleCode="Lrule Rrule Botrule"/> <th colspan="3" styleCode="Rrule Botrule"> <content styleCode="bold">Study 511</content> <content styleCode="bold">24 weeks</content> </th> <th colspan="2" styleCode="Rrule Botrule"> <content styleCode="bold">Study 542</content> <content styleCode="bold">48 weeks</content> </th> </tr> <tr styleCode="Botrule"> <th align="center" styleCode="Lrule Rrule"> Adverse Events </th> <th styleCode="Rrule">Placebo + ZDV/3TC (n=101)</th> <th styleCode="Rrule">500 mg TID VIRACEPT + ZDV/3TC (n=97)</th> <th styleCode="Rrule">750 mg TID VIRACEPT + ZDV/3TC (n=100)</th> <th styleCode="Rrule">1250 mg BID VIRACEPT + d4T/3TC (n=344)</th> <th styleCode="Rrule">750 mg TID VIRACEPT + d4T/3TC (n=210)</th> </tr> </thead> <tbody> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule">Digestive System</td> <td/> <td styleCode="Lrule Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Diarrhea</td> <td styleCode="Rrule">3%</td> <td styleCode="Rrule">14%</td> <td styleCode="Rrule">20%</td> <td styleCode="Rrule">20%</td> <td styleCode="Rrule">15%</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Nausea</td> <td styleCode="Rrule">4%</td> <td styleCode="Rrule">3%</td> <td styleCode="Rrule">7%</td> <td styleCode="Rrule">3%</td> <td styleCode="Rrule">3%</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Flatulence</td> <td styleCode="Rrule">0</td> <td styleCode="Rrule">5%</td> <td styleCode="Rrule">2%</td> <td styleCode="Rrule">1%</td> <td styleCode="Rrule">1%</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule">Skin/Appendages</td> <td/> <td styleCode="Lrule Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr> <td styleCode="Lrule Rrule"> Rash</td> <td styleCode="Rrule">1%</td> <td styleCode="Rrule">1%</td> <td styleCode="Rrule">3%</td> <td styleCode="Rrule">2%</td> <td styleCode="Rrule">1%</td> </tr> </tbody> </table>
adverse reactions table
<table width="100%"> <caption>Table 13 Percentage of Patients by Treatment Group With Marked Laboratory Abnormalities <footnote>Marked laboratory abnormalities are defined as a shift from Grade 0 at baseline to at least Grade 3 or from Grade 1 to Grade 4</footnote> in > 2% of Patients</caption> <col align="left" width="17%"/> <col align="center" width="16%"/> <col align="center" width="17%"/> <col align="center" width="16%"/> <col align="center" width="17%"/> <col align="center" width="17%"/> <thead> <tr> <th styleCode="Lrule Rrule Botrule"/> <th colspan="3" styleCode="Rrule Botrule">Study 511</th> <th colspan="2" styleCode="Rrule Botrule">Study 542 </th> </tr> <tr styleCode="Botrule"> <th align="center" styleCode="Lrule Rrule" valign="bottom"/> <th styleCode="Rrule" valign="bottom">Placebo + ZDV/3TC (n=101)</th> <th styleCode="Rrule" valign="bottom">500 mg TID VIRACEPT + ZDV/3TC (n=97)</th> <th styleCode="Rrule" valign="bottom">750 mg TID VIRACEPT + ZDV/3TC (n=100)</th> <th styleCode="Rrule" valign="bottom">1250 mg BID VIRACEPT + d4T/3TC (n=344)</th> <th styleCode="Rrule" valign="bottom">750 mg TID VIRACEPT + d4T/3TC (n=210)</th> </tr> </thead> <tbody> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule">Hematology</td> <td styleCode="Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Hemoglobin</td> <td styleCode="Rrule">6%</td> <td styleCode="Rrule">3%</td> <td styleCode="Rrule">2%</td> <td styleCode="Rrule">0</td> <td styleCode="Rrule">0</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Neutrophils</td> <td styleCode="Rrule">4%</td> <td styleCode="Rrule">3%</td> <td styleCode="Rrule">5%</td> <td styleCode="Rrule">2%</td> <td styleCode="Rrule">1%</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> Lymphocytes</td> <td styleCode="Rrule">1%</td> <td styleCode="Rrule">6%</td> <td styleCode="Rrule">1%</td> <td styleCode="Rrule">1%</td> <td styleCode="Rrule">0</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule">Chemistry</td> <td styleCode="Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> <td styleCode="Rrule"/> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> ALT (SGPT)</td> <td styleCode="Rrule">6%</td> <td styleCode="Rrule">1%</td> <td styleCode="Rrule">1%</td> <td styleCode="Rrule">2%</td> <td styleCode="Rrule">1%</td> </tr> <tr styleCode="Botrule"> <td styleCode="Lrule Rrule"> AST (SGOT)</td> <td styleCode="Rrule">4%</td> <td styleCode="Rrule">1%</td> <td styleCode="Rrule">0</td> <td styleCode="Rrule">2%</td> <td styleCode="Rrule">1%</td> </tr> <tr> <td styleCode="Lrule Rrule"> Creatine Kinase</td> <td styleCode="Rrule">7%</td> <td styleCode="Rrule">2%</td> <td styleCode="Rrule">2%</td> <td styleCode="Rrule">NA</td> <td styleCode="Rrule">NA</td> </tr> </tbody> </table>
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.