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
127193081 12719308 1 I 20160826 20160907 20160907 EXP NL-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-073485 BRISTOL MYERS SQUIBB 13.00 YR F Y 0.00000 20160907 OT NL NL

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
127193081 12719308 1 PS DIDANOSINE. DIDANOSINE 1 Unknown U 20156

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127193081 12719308 1 Perinatal HIV infection

Outcome of event

Event ID CASEID OUTC COD
127193081 12719308 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127193081 12719308 Gastric varices haemorrhage
127193081 12719308 Non-cirrhotic portal hypertension

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

no results found

Therapies reported

no results found