Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Saquinavir mesylate
Drug ID BADD_D01989
Description Saquinavir is an HIV-1 protease inhibitor used in combination with [ritonavir] and other antiretrovirals for the treatment of human immunodeficiency virus-1 (HIV-1) infection. In 1995 it became the first protease inhibitor approved by the FDA, followed shortly by ritonavir in 1996, and remains in clinical use today due to a relatively benign adverse effect profile as compared to other antiretroviral therapies.[A214382] While its efficacy was initially limited by exceptionally poor oral bioavailability (approximately 4%),[L3450] its current indications require the co-administration of ritonavir - a potent enzyme inhibitor - that increases the bioavailability and subsequent serum concentrations of saquinavir, thus dramatically improving antiviral activity.[A214382,L3450,L14351]
Indications and Usage Saquinavir is indicated, in combination with ritonavir and other antiretroviral agents, for the treatment of HIV-1 infection in patients 16 years of age and older.[L3450]
Marketing Status approved; investigational
ATC Code J05AE01
DrugBank ID DB01232
KEGG ID D01160
MeSH ID D019258
PubChem ID 60934
TTD Drug ID D0WI3T
NDC Product Code 0004-0244
UNII UHB9Z3841A
Synonyms Saquinavir | Saquinivir | Ro 31-8959 | Ro 31 8959 | Ro 318959 | Saquinavir Monomethanesulfonate | Monomethanesulfonate, Saquinavir | Saquinavir Mesylate | Invirase
Chemical Information
Molecular Formula C39H54N6O8S
CAS Registry Number 149845-06-7
SMILES CC(C)(C)NC(=O)C1CC2CCCCC2CN1CC(C(CC3=CC=CC=C3)NC(=O)C(CC(=O)N)NC(=O)C4=NC5=CC=CC =C5C=C4)O.CS(=O)(=O)O
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Euphoric mood19.04.02.006--
Eye disorder06.08.03.001--Not Available
Eye irritation06.04.05.003--Not Available
Facial pain08.01.08.012--
Factor XI deficiency03.15.01.005; 01.01.01.008--Not Available
Faeces discoloured07.01.03.002--Not Available
Fat tissue increased08.01.03.009--Not Available
Fatigue08.01.01.002--
Feeling abnormal08.01.09.014--Not Available
Flatulence07.01.04.002--
Folliculitis23.11.04.003; 11.02.01.053--
Frequent bowel movements07.02.04.002--Not Available
Fungal infection11.03.05.001--Not Available
Furuncle11.02.05.008; 23.11.02.009--Not Available
Gamma-glutamyltransferase increased13.03.04.024--
Gastritis07.08.02.001--
Gastrooesophageal reflux disease07.02.02.003--
Gastrointestinal disorder07.11.01.001--Not Available
Gastrointestinal haemorrhage24.07.02.009; 07.12.02.001--Not Available
Gastrointestinal pain07.01.05.005--
Gingivitis07.09.10.002; 11.01.04.013--
Glossitis07.14.01.001--Not Available
Haemarthrosis24.07.01.046; 15.01.01.004; 12.04.03.001--Not Available
Haematochezia24.07.02.012; 07.12.02.003--Not Available
Haematoma24.07.01.001--
Haemoglobin13.01.05.018--Not Available
Haemoglobin decreased13.01.05.003--Not Available
Haemolytic anaemia01.06.03.002--Not Available
Haemoptysis02.11.04.009; 24.07.01.006; 22.02.03.004--Not Available
Haemorrhage intracranial17.08.01.008; 24.07.04.003--
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