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
118649032 11864903 2 F 20000418 20160826 20151223 20160826 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-10859304 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160826 OT US FR

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
118649032 11864903 1 PS ZERIT STAVUDINE 1 Oral UNK Y 20412 CAPSULE, HARD
118649032 11864903 2 SS VIDEX DIDANOSINE 1 Oral UNK U 0
118649032 11864903 3 SS RETROVIR ZIDOVUDINE 1 Oral UNK Y 0
118649032 11864903 4 SS VIRACEPT NELFINAVIR MESYLATE 1 Oral 250 MG, UNK U 0 250 MG
118649032 11864903 5 SS NEVIRAPINE. NEVIRAPINE 1 Oral UNK U 0
118649032 11864903 6 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118649032 11864903 1 HIV test positive
118649032 11864903 2 HIV test positive
118649032 11864903 3 HIV test positive
118649032 11864903 4 HIV test positive
118649032 11864903 5 HIV test positive
118649032 11864903 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118649032 11864903 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118649032 11864903 Caesarean section
118649032 11864903 Dyspnoea
118649032 11864903 Metrorrhagia
118649032 11864903 Pregnancy
118649032 11864903 Tachycardia

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
118649032 11864903 5 20000418 20000418 0