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
123891712 12389171 2 F 2016 20160805 20160520 20160811 EXP BR-PFIZER INC-2016164508 PFIZER 58.00 YR M Y 65.00000 KG 20160811 CN BR BR

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
123891712 12389171 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG IN THE MORNING, CYCLIC 4X2 084BA 21938 50 MG CAPSULE, HARD
123891712 12389171 2 C LOSARTAN. LOSARTAN 1 50 MG 1 TABLET 1X DAILY 0 50 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123891712 12389171 1 Metastatic renal cell carcinoma
123891712 12389171 2 Hypertension

Outcome of event

Event ID CASEID OUTC COD
123891712 12389171 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123891712 12389171 Abasia
123891712 12389171 Anaemia
123891712 12389171 Asthenia
123891712 12389171 Disease progression
123891712 12389171 Dysstasia
123891712 12389171 Feeling abnormal
123891712 12389171 Metastatic renal cell carcinoma
123891712 12389171 Syncope

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
123891712 12389171 1 20160310 0