The Safety Rates Drug Report

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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
126533711 12653371 1 I 20160725 20160811 20160815 20160815 EXP GB-ABBVIE-16P-167-1701675-00 ABBVIE 34.00 YR F Y 0.00000 20160815 OT COUNTRY NOT SPECIFIED GB

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
126533711 12653371 1 PS RITONAVIR. RITONAVIR 1 Oral 1 COURSE FIRST TRIMESTER EARLIEST EXPOSURE, PRIOR TO CONCEPTION UNKNOWN 20945 100 MG SOFT CAPSULE QD
126533711 12653371 2 SS REYATAZ ATAZANAVIR SULFATE 1 Oral 1 COURSE FIRST TRIMESTER EARLIEST EXPOSURE, PRIOR TO CONCEPTION UNKNOWN 0 300 MG QD
126533711 12653371 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 COURSE (TAB/CAPS) FIRST TRIMESTER EARLIEST EXPOSURE, PRIOR TO CONCEPTION UNKNOWN 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126533711 12653371 1 Antiretroviral therapy
126533711 12653371 2 Antiretroviral therapy
126533711 12653371 3 Antiretroviral therapy

Outcome of event

Event ID CASEID OUTC COD
126533711 12653371 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126533711 12653371 Abortion spontaneous
126533711 12653371 Exposure during pregnancy
126533711 12653371 Foetal death

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

no results found

Therapies reported

no results found