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
125692111 12569211 1 I 20160531 20160705 20160719 20160719 EXP CH-SM-2016-05629 PHHY2016CH093628 NOVARTIS 47.90 YR M Y 90.00000 KG 20160719 OT 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
125692111 12569211 1 PS COSENTYX SECUKINUMAB 1 Subcutaneous 150 MG, QW 300 MG Y 125504 150 MG INJECTION /wk
125692111 12569211 2 SS IRFEN IBUPROFEN 1 Oral 800 MG, BID Y 0 800 MG BID
125692111 12569211 3 SS CRESTOR ROSUVASTATIN CALCIUM 1 Oral 20 MG, QD 0 20 MG QD
125692111 12569211 4 C PANTOZOL PANTOPRAZOLE SODIUM 1 Oral Y 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125692111 12569211 1 Spondylitis
125692111 12569211 2 Back pain
125692111 12569211 3 Hypercholesterolaemia
125692111 12569211 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125692111 12569211 HO
125692111 12569211 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125692111 12569211 Off label use
125692111 12569211 Pancreatitis necrotising
125692111 12569211 Portal vein thrombosis
125692111 12569211 Splenic thrombosis

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
125692111 12569211 1 20160531 20160607 0
125692111 12569211 2 201602 20160614 0
125692111 12569211 4 20160614 0