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
127233641 12723364 1 I 20160830 20160908 20160908 EXP CO-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-073617 BRISTOL MYERS SQUIBB 60.00 YR M Y 0.00000 20160908 OT CO CO

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
127233641 12723364 1 PS EFAVIRENZ EFAVIRENZ 1 Unknown U 20972
127233641 12723364 2 SS ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral UNK MG, UNK U 0 TABLET
127233641 12723364 3 C TENOFOVIR TENOFOVIR 1 Unknown U 0
127233641 12723364 4 C EMTRICITABINE EMTRICITABINE 1 Unknown U 0
127233641 12723364 5 C SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127233641 12723364 1 HIV infection
127233641 12723364 2 HIV infection
127233641 12723364 3 HIV infection
127233641 12723364 4 HIV infection
127233641 12723364 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127233641 12723364 DE
127233641 12723364 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127233641 12723364 Hepatic cirrhosis

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

no results found

Therapies reported

no results found