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
97870852 9787085 2 F 20091229 20151204 20131228 20160831 EXP GB-ROCHE-1324556 ROCHE 76.00 YR M 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
97870852 9787085 1 PS CAPECITABINE. CAPECITABINE 1 Oral TWICE DAILY ON DAYS 1-21 20896
97870852 9787085 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) OVER 30 MINUTES ON DAYS 1, 8 AND 15 U 0
97870852 9787085 3 C BISOPROLOL BISOPROLOL 1 0
97870852 9787085 4 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 0
97870852 9787085 5 C ESOMEPRAZOLE ESOMEPRAZOLE 1 0
97870852 9787085 6 C PARACETAMOL ACETAMINOPHEN 1 0
97870852 9787085 7 C ADCAL-D3 CALCIUM CARBONATECHOLECALCIFEROL 1 0
97870852 9787085 8 C RAMIPRIL. RAMIPRIL 1 0
97870852 9787085 9 C SIMVASTATIN. SIMVASTATIN 1 0
97870852 9787085 10 C DEXAMETHASONE. DEXAMETHASONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97870852 9787085 1 Pancreatic carcinoma
97870852 9787085 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
97870852 9787085 DE
97870852 9787085 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97870852 9787085 Abdominal distension
97870852 9787085 Constipation
97870852 9787085 Fatigue
97870852 9787085 General physical health deterioration
97870852 9787085 Peripheral swelling

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

no results found

Therapies reported

no results found