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
97870722 9787072 2 F 20100406 20151204 20131228 20160901 EXP GB-ROCHE-1326717 ROCHE 44.00 YR F Y 0.00000 20160901 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
97870722 9787072 1 PS CAPECITABINE. CAPECITABINE 1 Oral ON DAYS 1-21 U 20896 TABLET BID
97870722 9787072 2 SS GEMCITABINE HYDROCHLORIDE. GEMCITABINE HYDROCHLORIDE 1 Intravenous (not otherwise specified) OVER 30 MINUTES ON DAYS 1, 8, AND 15 U 0
97870722 9787072 3 C PARACETAMOL ACETAMINOPHEN 1 0
97870722 9787072 4 C OMEPRAZOLE. OMEPRAZOLE 1 0
97870722 9787072 5 C FENTANYL. FENTANYL 1 0
97870722 9787072 6 C OXYNORM OXYCODONE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97870722 9787072 1 Pancreatic carcinoma
97870722 9787072 2 Pancreatic carcinoma

Outcome of event

Event ID CASEID OUTC COD
97870722 9787072 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97870722 9787072 Abdominal distension
97870722 9787072 Anaemia
97870722 9787072 Cholangitis
97870722 9787072 Pyrexia

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

no results found

Therapies reported

no results found