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
125541391 12554139 1 I 20160531 20160705 20160713 20160713 EXP CH-ASTRAZENECA-2016SE73299 ASTRAZENECA 17494.00 DY M Y 90.00000 KG 20160713 MD CH CH

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
125541391 12554139 1 PS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 21366 20 MG TABLET QD
125541391 12554139 2 SS IRFEN IBUPROFEN 1 Oral 195200 MG Y U 0 800 MG BID
125541391 12554139 3 SS COSENTYX SECUKINUMAB 1 Subcutaneous U U 0 150 MG INJECTION /wk
125541391 12554139 4 SS COSENTYX SECUKINUMAB 1 Subcutaneous U U 0 150 MG INJECTION /wk
125541391 12554139 5 C PANTOZOL PANTOPRAZOLE SODIUM 1 Oral 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125541391 12554139 1 Hypercholesterolaemia
125541391 12554139 2 Back pain
125541391 12554139 3 Spondylitis
125541391 12554139 4 Spondylitis

Outcome of event

Event ID CASEID OUTC COD
125541391 12554139 HO
125541391 12554139 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125541391 12554139 Off label use
125541391 12554139 Pancreatitis necrotising
125541391 12554139 Portal vein thrombosis
125541391 12554139 Splenic thrombosis
125541391 12554139 Steatohepatitis

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
125541391 12554139 2 201602 20160614 0
125541391 12554139 3 20160531 0
125541391 12554139 4 20160607 0
125541391 12554139 5 20160614 0