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
121412574 12141257 4 F 20160705 20160303 20160714 EXP BR-PFIZER INC-2016118636 PFIZER 68.00 YR M Y 0.00000 20160714 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
121412574 12141257 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG, CYCLE 2X1, (CONTINUOUS USE IN ALTERNATED DAYS) (ONCE DAILY) U Z597A 21938 50 MG CAPSULE, HARD
121412574 12141257 2 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 UNK 0
121412574 12141257 3 C LASIX FUROSEMIDE 1 UNK 0
121412574 12141257 4 C ALENIA /01479302/ 2 UNK, 2X/DAY 0 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121412574 12141257 1 Metastatic renal cell carcinoma
121412574 12141257 2 Diverticulitis

Outcome of event

Event ID CASEID OUTC COD
121412574 12141257 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121412574 12141257 Dyspnoea
121412574 12141257 Herpes virus infection
121412574 12141257 Thyroid disorder
121412574 12141257 Weight decreased

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
121412574 12141257 1 20150826 0