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
119715652 11971565 2 F 20151219 20160131 20160128 20160801 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-003763 BRISTOL MYERS SQUIBB 26.00 YR F Y 0.00000 20160801 CN 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
119715652 11971565 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Oral 400 MG, QD 21567 400 MG QD
119715652 11971565 2 SS NORVIR RITONAVIR 1 Oral 100 MG, QD 0 100 MG QD
119715652 11971565 3 SS LAMIVUDINE AND ZIDOVUDINE LAMIVUDINEIDOVUDINE 1 Oral 1 DF, UNK 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119715652 11971565 1 HIV infection
119715652 11971565 2 HIV infection
119715652 11971565 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
119715652 11971565 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119715652 11971565 Maternal exposure during pregnancy
119715652 11971565 Stillbirth

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
119715652 11971565 1 20151028 0
119715652 11971565 2 20151028 0
119715652 11971565 3 20151028 0