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
125496982 12549698 2 F 20160509 20160701 20160712 20160714 EXP FR-PFIZER INC-2016323823 PFIZER 61.00 YR F Y 0.00000 20160714 OT FR FR

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
125496982 12549698 1 PS SUTENT SUNITINIB MALATE 1 50 MG, 1X/DAY 600 MG 21938 50 MG CAPSULE, HARD QD
125496982 12549698 2 SS HYDROCORTISONE. HYDROCORTISONE 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125496982 12549698 1 Clear cell renal cell carcinoma
125496982 12549698 2 Adrenal insufficiency

Outcome of event

Event ID CASEID OUTC COD
125496982 12549698 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125496982 12549698 Adrenocortical insufficiency acute
125496982 12549698 Coma
125496982 12549698 Diarrhoea
125496982 12549698 Disseminated intravascular coagulation
125496982 12549698 General physical health deterioration
125496982 12549698 Haemoconcentration
125496982 12549698 Hyperkalaemia
125496982 12549698 Hypoglycaemia
125496982 12549698 Hyponatraemia
125496982 12549698 Hypotension
125496982 12549698 Pyrexia
125496982 12549698 Renal failure

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
125496982 12549698 1 20160502 20160513 0
125496982 12549698 2 201601 0