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
119090722 11909072 2 F 19980407 20160826 20160112 20160827 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2006-000021 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160827 CN FR 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
119090722 11909072 1 PS ZERIT STAVUDINE 1 Unknown UNK U 20412
119090722 11909072 2 SS EPIVIR LAMIVUDINE 1 Unknown UNK U 0
119090722 11909072 3 SS RIFADINE RIFAMPIN 1 Unknown UNK U 0
119090722 11909072 4 SS RIMIFON ISONIAZID 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119090722 11909072 1 HIV infection
119090722 11909072 2 HIV infection
119090722 11909072 3 Pulmonary tuberculosis
119090722 11909072 4 Pulmonary tuberculosis

Outcome of event

Event ID CASEID OUTC COD
119090722 11909072 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119090722 11909072 Caesarean section
119090722 11909072 Live birth
119090722 11909072 Maternal exposure during pregnancy
119090722 11909072 Meconium in amniotic fluid

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

no results found

Therapies reported

no results found