The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125808932 12580893 2 F 201606 20160719 20160721 20160726 EXP GB-ABBVIE-16K-167-1665173-00 ABBVIE 49.31 YR M Y 0.00000 20160726 CN GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125808932 12580893 1 PS NORVIR RITONAVIR 1 Oral U UNKNOWN 22417 100 MG TABLET
125808932 12580893 2 SS RALTEGRAVIR. RALTEGRAVIR 1 Oral U UNKNOWN 0 400 MG TABLET
125808932 12580893 3 SS DARUNAVIR DARUNAVIR 1 Oral U UNKNOWN 0 800 MG TABLET
125808932 12580893 4 SS TENOFOVIR DISOPROXIL FUMARATE. TENOFOVIR DISOPROXIL FUMARATE 1 Oral U UNKNOWN 0 245 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125808932 12580893 1 HIV infection
125808932 12580893 2 HIV infection
125808932 12580893 3 HIV infection
125808932 12580893 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125808932 12580893 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125808932 12580893 Activities of daily living impaired
125808932 12580893 Hypersomnia
125808932 12580893 Malaise
125808932 12580893 Seizure
125808932 12580893 Viral load increased
125808932 12580893 Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found