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
97875252 9787525 2 F 20080812 20151204 20131230 20160829 EXP GB-ROCHE-1326722 ROCHE 67.00 YR F Y 0.00000 20160829 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
97875252 9787525 1 PS CAPECITABINE. CAPECITABINE 1 Oral ON DAYS 1-21 U 20896 TABLET BID
97875252 9787525 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) 30 MINUTES ON DAYS 1, 8, AND 15 U 0
97875252 9787525 3 SS SARGRAMOSTIM SARGRAMOSTIM 1 Intradermal U 0
97875252 9787525 4 C ENOXAPARIN ENOXAPARIN 1 0
97875252 9787525 5 C ATENOLOL. ATENOLOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97875252 9787525 1 Pancreatic carcinoma
97875252 9787525 2 Pancreatic carcinoma
97875252 9787525 3 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
97875252 9787525 DE
97875252 9787525 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97875252 9787525 Abdominal pain
97875252 9787525 Blood albumin decreased
97875252 9787525 Confusional state
97875252 9787525 Decreased appetite
97875252 9787525 Device occlusion
97875252 9787525 Dyspnoea
97875252 9787525 Hypercalcaemia
97875252 9787525 Nausea
97875252 9787525 Oedema

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

no results found

Therapies reported

no results found