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
124903563 12490356 3 F 20160613 20160708 20160622 20160714 EXP MW-GILEAD-2016-0219942 GILEAD 38.00 YR A M Y 0.00000 20160714 MD MW MW

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
124903563 12490356 1 PS EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1100 MG, QD 364100 MG 21937 1100 MG TABLET QD
124903563 12490356 2 SS EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 364100 MG 21937 TABLET
124903563 12490356 3 SS BLEOMYCIN BLEOMYCIN SULFATE 1 Intravenous (not otherwise specified) 15 IU, Q3WK 75 IU 0 15 IU Q3W
124903563 12490356 4 SS VINCRISTINE VINCRISTINE 1 Intravenous (not otherwise specified) 2 MG, Q3WK 10 MG 0 2 MG Q3W

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124903563 12490356 1 Acquired immunodeficiency syndrome
124903563 12490356 2 Kaposi's sarcoma
124903563 12490356 3 Chemotherapy
124903563 12490356 4 Chemotherapy

Outcome of event

Event ID CASEID OUTC COD
124903563 12490356 HO
124903563 12490356 LT
124903563 12490356 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124903563 12490356 Anaemia
124903563 12490356 Bacterial sepsis
124903563 12490356 Disseminated tuberculosis

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
124903563 12490356 1 20150717 20160612 0
124903563 12490356 3 20150901 20151224 0
124903563 12490356 4 20150901 20151224 0