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
127982791 12798279 1 I 20160218 20160923 20160930 20160930 EXP FR-JNJFOC-20160923806 JANSSEN 83.00 YR E M Y 0.00000 20160930 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
127982791 12798279 1 PS ZYTIGA ABIRATERONE ACETATE 1 Oral Y N 202379 TABLET
127982791 12798279 2 SS FUROSEMIDE. FUROSEMIDE 1 Oral Y 0 50 MG UNSPECIFIED
127982791 12798279 3 SS INDAPAMIDE. INDAPAMIDE 1 Oral Y 0 50 MG TABLET
127982791 12798279 4 C LEVEMIR INSULIN DETEMIR 1 Unknown D 0 UNSPECIFIED
127982791 12798279 5 C KALEORID POTASSIUM CHLORIDE 1 Unknown D 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127982791 12798279 1 Prostate cancer
127982791 12798279 2 Hypertension
127982791 12798279 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127982791 12798279 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127982791 12798279 Cardiac disorder
127982791 12798279 Hypokalaemia
127982791 12798279 Ischaemic stroke

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
127982791 12798279 1 20160220 0
127982791 12798279 2 20160218 0
127982791 12798279 3 20160219 0