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
125840701 12584070 1 I 20160316 20160718 20160722 20160722 EXP US-ABBVIE-16P-163-1680695-00 ABBVIE 23.00 YR F Y 0.00000 20160722 OT COUNTRY NOT SPECIFIED 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
125840701 12584070 1 PS RITONAVIR. RITONAVIR 1 Oral UNKNOWN 20945 100 MG SOFT CAPSULE QD
125840701 12584070 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 0 1 DF TABLET QD
125840701 12584070 3 SS PREZISTA DARUNAVIR ETHANOLATE 1 Oral 0 2 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125840701 12584070 1 HIV infection
125840701 12584070 2 HIV infection
125840701 12584070 3 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125840701 12584070 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125840701 12584070 Abortion induced
125840701 12584070 Exposure during pregnancy
125840701 12584070 Foetal death

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
125840701 12584070 1 20151215 0
125840701 12584070 2 20151215 0
125840701 12584070 3 20151215 0