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
122249267 12224926 7 F 20160420 20160627 20160331 20160706 EXP US-PFIZER INC-2016172738 PFIZER 71.00 YR M Y 72.00000 KG 20160706 CN 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
122249267 12224926 1 PS SUTENT SUNITINIB MALATE 1 37.5 MG, CYCLIC (28 DAYS ON/14 DAYS OFF) 21938 37.5 MG CAPSULE, HARD
122249267 12224926 2 C ASPIRIN /00002701/ ASPIRIN 1 UNK 0
122249267 12224926 3 C AMARYL GLIMEPIRIDE 1 UNK 0
122249267 12224926 4 C VITAMIN B12 CYANOCOBALAMIN 1 UNK 0
122249267 12224926 5 C KEPPRA LEVETIRACETAM 1 UNK 0
122249267 12224926 6 C COLACE DOCUSATE SODIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122249267 12224926 1 Metastatic renal cell carcinoma

Outcome of event

Event ID CASEID OUTC COD
122249267 12224926 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
122249267 12224926 Asthenia
122249267 12224926 Blood calcium decreased
122249267 12224926 Blood glucose decreased
122249267 12224926 Blood pressure increased
122249267 12224926 Death
122249267 12224926 Decreased appetite
122249267 12224926 Dry skin
122249267 12224926 Dysarthria
122249267 12224926 Fatigue
122249267 12224926 Hypersomnia
122249267 12224926 Irritability
122249267 12224926 Lacrimation increased
122249267 12224926 Memory impairment
122249267 12224926 Tremor

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
122249267 12224926 1 20160311 20160525 0