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
118851072 11885107 2 F 200111 20160825 20160104 20160825 EXP US-BRISTOL-MYERS SQUIBB COMPANY-11769163 BRISTOL MYERS SQUIBB 34.00 YR F Y 0.00000 20160825 OT US US

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
118851072 11885107 1 PS STAVUDINE. STAVUDINE 1 Oral 80 MG, QD 20412 80 MG QD
118851072 11885107 2 SS ZIAGEN ABACAVIR SULFATE 1 Oral 600 MG, QD 0 600 MG QD
118851072 11885107 3 SS EPIVIR LAMIVUDINE 1 Oral 30 MG, QD 0 30 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118851072 11885107 1 HIV infection
118851072 11885107 2 HIV infection
118851072 11885107 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
118851072 11885107 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118851072 11885107 Abortion induced
118851072 11885107 Foetal death
118851072 11885107 Pregnancy
118851072 11885107 Retroplacental haematoma

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
118851072 11885107 1 20010701 0
118851072 11885107 2 20010701 0
118851072 11885107 3 20010701 0