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
123109736 12310973 6 F 20160420 20160810 20160427 20160816 PER US-PFIZER INC-2016229286 PFIZER 69.00 YR F Y 57.00000 KG 20160816 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
123109736 12310973 1 PS SUTENT SUNITINIB MALATE 1 50 MG, UNK Y 21938 50 MG CAPSULE, HARD
123109736 12310973 2 SS SUTENT SUNITINIB MALATE 1 25 MG, CYCLIC (2 WEEKS ON/1 WEEK OFF) Y 21938 25 MG CAPSULE, HARD
123109736 12310973 3 C AMLODIPINE AMLODIPINE BESYLATE 1 10 MG, 1X/DAY 0 10 MG QD
123109736 12310973 4 C LIPITOR ATORVASTATIN CALCIUM 1 20 MG, 1X/DAY 0 20 MG QD
123109736 12310973 5 C VITAMIN D CHOLECALCIFEROL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123109736 12310973 1 Renal cancer metastatic
123109736 12310973 3 Blood pressure abnormal
123109736 12310973 4 Blood cholesterol increased

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123109736 12310973 Blood potassium decreased
123109736 12310973 Decreased appetite
123109736 12310973 Malaise
123109736 12310973 Musculoskeletal pain
123109736 12310973 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
123109736 12310973 1 201511 201602 0
123109736 12310973 2 201602 20160708 0
123109736 12310973 5 20160622 0