The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
8480333 8525904 I 8480333-2 20120322 20120620 20120630 EXP GB-TEVA-344257ISR TEVA 62 YR F Y 61.5 KG 20120630 MD UNITED KINGDOM

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
8480333 1020135250 C AMLODIPINE 1 ORAL 5 MILLIGRAM;
8480333 1020135249 C CO-DYDRAMOL 2 ORAL
8480333 1020135246 SS AVASTIN 1 INTRAVENOUS
8480333 1020135245 PS IRINOTECAN HCL 1 INTRAVENOUS 077260
8480333 1020135251 C LANSOPRAZOLE 1 ORAL 30 MILLIGRAM;
8480333 1020135247 SS FLUOROURACIL 1 INTRAVENOUS BOLUS
8480333 1020135248 SS FLUOROURACIL 1 OVER 48 HRS

Indications of drugs used

Event ID DRUG SEQ INDI PT
8480333 1020135250 HYPERTENSION
8480333 1020135249 PAIN
8480333 1020135246 COLON CANCER METASTATIC
8480333 1020135245 COLON CANCER METASTATIC
8480333 1020135251 DYSPEPSIA
8480333 1020135247 COLON CANCER METASTATIC

Outcome of event

Event ID OUTC COD
8480333 OT
8480333 DE
8480333 HO

Reactions reported

Event ID PT
8480333 UPPER GASTROINTESTINAL HAEMORRHAGE
8480333 SMALL INTESTINAL OBSTRUCTION
8480333 PULMONARY EMBOLISM
8480333 HYPOTENSION

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
8480333 1020135246 20111115 20120313
8480333 1020135247 20111101 20120313 134 DAY
8480333 1020135248 134 DAY