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
127229661 12722966 1 I 20160831 20160908 20160908 EXP US-CIPLA LTD.-2016US17999 CIPLA 0.00 Y 0.00000 20160908 OT 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
127229661 12722966 1 PS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Unknown UNK U U 78759 INFUSION
127229661 12722966 2 SS CISPLATIN. CISPLATIN 1 Unknown UNK U U 0
127229661 12722966 3 SS CAPECITABINE. CAPECITABINE 1 Unknown UNK U U 0
127229661 12722966 4 SS FLUOROURACIL. FLUOROURACIL 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127229661 12722966 1 Gallbladder adenocarcinoma
127229661 12722966 2 Gallbladder adenocarcinoma
127229661 12722966 3 Gallbladder adenocarcinoma
127229661 12722966 4 Gallbladder adenocarcinoma

Outcome of event

Event ID CASEID OUTC COD
127229661 12722966 DE
127229661 12722966 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127229661 12722966 Chromosomal deletion
127229661 12722966 Disease progression
127229661 12722966 Dysplasia
127229661 12722966 Thrombocytopenia

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

no results found

Therapies reported

no results found