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
680694210 6806942 10 F 20080422 20160824 20081110 20160824 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-14017800 BRISTOL MYERS SQUIBB 32.31 YR F Y 68.00000 KG 20160824 CN GB 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
680694210 6806942 1 PS SUSTIVA EFAVIRENZ 1 Oral 1 DF, UNK Y 20972 1 DF CAPSULE
680694210 6806942 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, UNK U 0 1 DF
680694210 6806942 3 C FUMAFER FERROUS FUMARATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
680694210 6806942 1 Antiretroviral therapy
680694210 6806942 2 Antiretroviral therapy
680694210 6806942 3 Iron deficiency

Outcome of event

Event ID CASEID OUTC COD
680694210 6806942 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
680694210 6806942 Abortion induced
680694210 6806942 Maternal exposure during pregnancy

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
680694210 6806942 1 20051201 20071211 0
680694210 6806942 2 20051201 0
680694210 6806942 3 200711 0