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
127426811 12742681 1 I 20141015 20151126 20160914 20160914 EXP PHJP2015JP021350 NOVARTIS 66.00 YR F Y 0.00000 20160914 JP JP

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
127426811 12742681 1 PS VOTRIENT PAZOPANIB HYDROCHLORIDE 1 Oral 400 MG, QD Y 22465 400 MG FILM-COATED TABLET QD
127426811 12742681 2 SS VOTRIENT PAZOPANIB HYDROCHLORIDE 1 Oral 600 MG, QD Y 22465 600 MG FILM-COATED TABLET QD
127426811 12742681 3 SS PHENYTOIN. PHENYTOIN 1 Unknown UNK Y 0
127426811 12742681 4 SS LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127426811 12742681 1 Renal cancer
127426811 12742681 3 Seizure
127426811 12742681 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127426811 12742681 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127426811 12742681 Diarrhoea
127426811 12742681 Drug reaction with eosinophilia and systemic symptoms
127426811 12742681 Hepatic function abnormal
127426811 12742681 Pyrexia
127426811 12742681 Rash
127426811 12742681 White blood cell count increased

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127426811 12742681 1 20141006 0
127426811 12742681 2 20141015 20141029 0
127426811 12742681 3 20141031 0