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
97821752 9782175 2 F 20101115 20151204 20131226 20160831 EXP GB-ROCHE-1324946 ROCHE 76.00 YR F Y 0.00000 20160831 MD GB 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
97821752 9782175 1 PS CAPECITABINE. CAPECITABINE 1 Unknown U 20896
97821752 9782175 2 SS GEMCITABINE GEMCITABINEGEMCITABINE HYDROCHLORIDE 1 Unknown U 0
97821752 9782175 3 C COCODAMOL ACETAMINOPHENCODEINE PHOSPHATE 1 0
97821752 9782175 4 C SIMVASTATIN. SIMVASTATIN 1 0
97821752 9782175 5 C NICORANDIL NICORANDIL 1 0
97821752 9782175 6 C FUROSEMIDE. FUROSEMIDE 1 0
97821752 9782175 7 C PERINDOPRIL PERINDOPRIL 1 0
97821752 9782175 8 C ASPIRIN. ASPIRIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97821752 9782175 1 Pancreatic carcinoma
97821752 9782175 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
97821752 9782175 DE
97821752 9782175 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97821752 9782175 Anaemia
97821752 9782175 Biliary sepsis
97821752 9782175 Device occlusion
97821752 9782175 Infection
97821752 9782175 Pulmonary embolism
97821752 9782175 Thrombocytopenia

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

no results found

Therapies reported

no results found