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
125821421 12582142 1 I 20160708 20160722 20160722 EXP US-CIPLA LTD.-2016US09822 CIPLA 0.00 Y 0.00000 20160722 OT 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
125821421 12582142 1 PS CARBOPLATIN. CARBOPLATIN 1 Intra-arterial AUC 6, INFUSED FOR 30-45 MINS, EVERY SIX WEEKS CYCLE U 77383 INFUSION
125821421 12582142 2 SS CISPLATIN. CISPLATIN 1 Intra-arterial 60 MG/M2, INFUSED FOR 30-45 MINS, EVERY SIX WEEKS CYCLE U 0 60 MG/M**2 INFUSION
125821421 12582142 3 SS SORAFENIB SORAFENIB 1 Oral 400 MG, BID U 0 400 MG
125821421 12582142 4 SS SORAFENIB SORAFENIB 1 Oral 400 MG, DAILY U 0 400 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125821421 12582142 1 Hepatocellular carcinoma
125821421 12582142 2 Hepatocellular carcinoma
125821421 12582142 3 Hepatocellular carcinoma

Outcome of event

Event ID CASEID OUTC COD
125821421 12582142 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125821421 12582142 Hepatic encephalopathy

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

no results found

Therapies reported

no results found