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
127242561 12724256 1 I 20150317 0 20160903 20160903 DIR FDA-CTU 56.62 YR F N 86.36000 KG 20160831 N MD 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
127242561 12724256 1 PS CASODEX BICALUTAMIDE 1 0 2350 MG
127242561 12724256 2 SS LEUPROLIDE ACETATE. LEUPROLIDE ACETATE 1 0 37.5 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127242561 12724256 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127242561 12724256 Abdominal abscess
127242561 12724256 Acute kidney injury
127242561 12724256 Alanine aminotransferase increased
127242561 12724256 Anal incontinence
127242561 12724256 Aspartate aminotransferase increased
127242561 12724256 Colitis
127242561 12724256 Colon neoplasm
127242561 12724256 Dehydration
127242561 12724256 Diarrhoea
127242561 12724256 Diverticulitis
127242561 12724256 Haemoglobin decreased
127242561 12724256 Pelvic abscess
127242561 12724256 Platelet count increased
127242561 12724256 Small intestinal obstruction
127242561 12724256 White blood cell count increased

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
127242561 12724256 1 20150310 0
127242561 12724256 2 20150302 0