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
126038962 12603896 2 F 201603 20160805 20160728 20160809 EXP TH-PFIZER INC-2016333230 PFIZER 67.00 YR F Y 0.00000 20160809 CN TH TH

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
126038962 12603896 1 PS SUTENT SUNITINIB MALATE 1 Oral 50 MG (12.5 MGX4CAPSULES), DAILY Y 21938 50 MG CAPSULE, HARD
126038962 12603896 2 SS SUTENT SUNITINIB MALATE 1 Oral 12.5 MG, DAILY Y 21938 12.5 MG CAPSULE, HARD
126038962 12603896 3 SS SUTENT SUNITINIB MALATE 1 Oral 25 MG (12.5 MGX2 CAPSULES), DAILY Y 21938 25 MG CAPSULE, HARD
126038962 12603896 4 C AMLODIPINE BESILATE AMLODIPINE BESYLATE 1 UNK 0
126038962 12603896 5 C PROPANOLOL /00030001/ PROPRANOLOL HYDROCHLORIDE 1 UNK 0
126038962 12603896 6 C ASPIRIN /00002701/ ASPIRIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126038962 12603896 1 Metastatic renal cell carcinoma
126038962 12603896 4 Hypertension

Outcome of event

Event ID CASEID OUTC COD
126038962 12603896 DE
126038962 12603896 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126038962 12603896 Disease progression
126038962 12603896 Dysgeusia
126038962 12603896 Lip dry
126038962 12603896 Metastatic renal cell carcinoma
126038962 12603896 White blood cell count 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
126038962 12603896 1 201603 201603 0
126038962 12603896 2 201604 0
126038962 12603896 3 2016 0