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
73649854 7364985 4 F 20100331 20160823 20100423 20160916 EXP US-ROCHE-698743 ROCHE 65.00 YR M Y 93.20000 KG 20160916 MD US US

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
73649854 7364985 1 PS Bevacizumab BEVACIZUMAB 1 Intravenous (not otherwise specified) LAST ADMINISTERED DATE: 24 MARCH 2010OVER 30- 90 MINUTES ON DAYS 1 AND 15. CYCLE: 28 DAYS U 125085 935 MG SOLUTION FOR INFUSION
73649854 7364985 2 SS TEMSIROLIMUS TEMSIROLIMUS 1 Intravenous (not otherwise specified) LAST ADMINISTERED DATE: 24 MARCH 2010, ON DAYS 1, 8, 15 AND 22. CYCLE: 28 DAYS U 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
73649854 7364985 1 Hepatocellular carcinoma
73649854 7364985 2 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
73649854 7364985 HO
73649854 7364985 OT
73649854 7364985 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
73649854 7364985 Abdominal pain
73649854 7364985 Acute kidney injury
73649854 7364985 Metabolic acidosis
73649854 7364985 Multiple organ dysfunction syndrome
73649854 7364985 Nausea
73649854 7364985 Peritonitis
73649854 7364985 Renal failure
73649854 7364985 Respiratory failure

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

no results found

Therapies reported

no results found