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
124984732 12498473 2 F 20151101 20160627 20160627 20160706 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-050605 BRISTOL MYERS SQUIBB 31.00 YR F Y 0.00000 20160706 OT 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
124984732 12498473 1 PS ATAZANAVIR SULFATE ATAZANAVIR SULFATE 1 Unknown UNK U 21567
124984732 12498473 2 SS ABACAVIR + LAMIVUDIN ABACAVIRLAMIVUDINE 1 Unknown UNK U 0
124984732 12498473 3 SS EMTRICITABINE W/RILPIVIRINE/TENOFOVIR DISOPRO EMTRICITABINERILPIVIRINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, QD Y 0 1 DF QD
124984732 12498473 4 SS NORVIR RITONAVIR 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124984732 12498473 1 Antiretroviral therapy
124984732 12498473 2 Antiretroviral therapy
124984732 12498473 3 Antiretroviral therapy
124984732 12498473 4 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
124984732 12498473 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124984732 12498473 Abortion induced
124984732 12498473 Ectopic pregnancy
124984732 12498473 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
124984732 12498473 3 20150413 20150914 0