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
125945751 12594575 1 I 20160714 20160726 20160726 EXP PL-ACTAVIS-2016-16229 ACTAVIS SAWICKA E, MIRONCZUK A, WOJTUKIEWICZ MZ, SIERKO E. CHEMORADIOTHERAPY FOR LOCALLY ADVANCED PANCREATIC CANCER PATIENTS: IS IT STILL AN OPEN QUESTION?. CONTEMP ONCOL. 2016;20(2):102-108. 56.00 YR M Y 0.00000 20160726 MD PL PL

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
125945751 12594575 1 PS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 1800 MG, CYCLICAL (6.5 COURSES; ON DAYS 1, 8, AND 15 EVERY 4 WEEKS) UNCONFIRMED 79160 1800 MG UNK

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125945751 12594575 1 Ductal adenocarcinoma of pancreas

Outcome of event

Event ID CASEID OUTC COD
125945751 12594575 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125945751 12594575 Abdominal pain
125945751 12594575 Anaemia
125945751 12594575 Cardiac disorder
125945751 12594575 Diarrhoea
125945751 12594575 Leukopenia
125945751 12594575 Nausea
125945751 12594575 Pain
125945751 12594575 Thrombocytopenia
125945751 12594575 Vomiting
125945751 12594575 Weight increased

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

no results found

Therapies reported

no results found