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
98695594 9869559 4 F 20160707 20140205 20160728 PER US-PFIZER INC-2014031991 PFIZER 59.00 YR M Y 0.00000 20160728 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
98695594 9869559 1 PS SUTENT SUNITINIB MALATE 1 12.5 MG, UNK U 21938 12.5 MG CAPSULE, HARD
98695594 9869559 2 C ALLOPURINOL. ALLOPURINOL 1 UNK 0
98695594 9869559 3 C ASPIRIN. ASPIRIN 1 UNK 0
98695594 9869559 4 C COENZYME Q10 UBIDECARENONE 1 UNK 0
98695594 9869559 5 C CRESTOR ROSUVASTATIN CALCIUM 1 UNK 0
98695594 9869559 6 C FISH OIL FISH OIL 1 UNK 0
98695594 9869559 7 C VITAMIN D3 CHOLECALCIFEROL 1 UNK 0
98695594 9869559 8 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 UNK 0
98695594 9869559 9 C LOSARTAN POTASSIUM. LOSARTAN POTASSIUM 1 UNK 0
98695594 9869559 10 C CILOXAN CIPROFLOXACIN HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98695594 9869559 1 Renal cancer
98695594 9869559 8 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
98695594 9869559 Decreased appetite
98695594 9869559 Epistaxis
98695594 9869559 Palmar-plantar erythrodysaesthesia syndrome
98695594 9869559 Paraesthesia oral

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
98695594 9869559 1 20140107 0