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
125773892 12577389 2 F 20160521 20160810 20160720 20160818 EXP FR-ASTRAZENECA-2016SE75788 ASTRAZENECA 29977.00 DY M Y 0.00000 20160818 MD 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
125773892 12577389 1 PS CASODEX BICALUTAMIDE 1 Oral 102 DF 20498 1 DF TABLET QD
125773892 12577389 2 SS ESOMEPRAZOLE EG ESOMEPRAZOLE 1 Oral U 0 1 DF QD
125773892 12577389 3 SS DIFFU K POTASSIUM CHLORIDE 1 Oral U 0 1 DF QD
125773892 12577389 4 SS XTANDI ENZALUTAMIDE 1 Oral 160.0MG UNKNOWN 0 160 MG
125773892 12577389 5 SS LACTULOSE. LACTULOSE 1 Oral 0 2 DF QD
125773892 12577389 6 SS OXYNORMORO OXYCODONE 1 Oral 5 MG, IF NEEDED 0
125773892 12577389 7 SS BISOPROLOL EG BISOPROLOL 1 Oral 221.25 MG 0 1.25 MG QD
125773892 12577389 8 SS NICORANDIL NICORANDIL 1 Oral 0 1 DF QD
125773892 12577389 9 SS KARDEGIC ASPIRIN LYSINE 1 Oral 0 1 DF QD
125773892 12577389 10 SS PREDNISONE. PREDNISONE 1 Oral 0 1 MG QD
125773892 12577389 11 SS NORMACOL KARAYA GUM 1 Rectal IF NEED 0
125773892 12577389 12 SS PRAVASTATINE EG PRAVASTATIN SODIUM 1 Oral 0 1 DF QD
125773892 12577389 13 SS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 0 1 DF QD
125773892 12577389 14 SS DOLIPRANE ACETAMINOPHEN 1 Oral 1 G, IF NEED 0
125773892 12577389 15 SS OXYCONTIN OXYCODONE HYDROCHLORIDE 1 Oral 0 1 DF TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125773892 12577389 1 Prostate cancer
125773892 12577389 2 Gastrooesophageal reflux disease
125773892 12577389 3 Hypokalaemia
125773892 12577389 4 Prostate cancer
125773892 12577389 5 Constipation
125773892 12577389 6 Pain
125773892 12577389 7 Hypertension
125773892 12577389 8 Angina unstable
125773892 12577389 9 Cardiovascular event prophylaxis
125773892 12577389 10 Product used for unknown indication
125773892 12577389 11 Constipation
125773892 12577389 12 Hypercholesterolaemia
125773892 12577389 13 Diabetes mellitus
125773892 12577389 14 Pain
125773892 12577389 15 Pain

Outcome of event

Event ID CASEID OUTC COD
125773892 12577389 DE
125773892 12577389 HO
125773892 12577389 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125773892 12577389 Abdominal pain
125773892 12577389 Calculus urinary
125773892 12577389 Cholestasis
125773892 12577389 Hepatic encephalopathy
125773892 12577389 Hepatic function abnormal
125773892 12577389 Hepatorenal syndrome
125773892 12577389 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
125773892 12577389 1 20160210 0
125773892 12577389 2 20160606 0
125773892 12577389 3 20160528 20160606 0
125773892 12577389 4 20160524 0
125773892 12577389 5 20160528 0
125773892 12577389 6 20160526 0
125773892 12577389 7 20151127 0
125773892 12577389 10 20160606 0
125773892 12577389 11 20160507 0
125773892 12577389 12 20160606 0
125773892 12577389 13 20160606 0
125773892 12577389 15 20160526 0