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
125292471 12529247 1 I 20160701 20160705 20160705 EXP AU-BAUSCH-BL-2016-015680 BAUSCH AND LOMB 57.00 YR M Y 0.00000 20160705 OT AU AU

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
125292471 12529247 1 PS PREDNISOLONE. PREDNISOLONE 1 Unknown U 40070
125292471 12529247 2 SS VIEKIRA PAK DASABUVIROMBITASVIRPARITAPREVIRRITONAVIR 1 Unknown U 0
125292471 12529247 3 C INSULIN INSULIN NOS 1 0
125292471 12529247 4 C MESALAZINE MESALAMINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125292471 12529247 1 Product used for unknown indication
125292471 12529247 2 Product used for unknown indication
125292471 12529247 3 Product used for unknown indication
125292471 12529247 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125292471 12529247 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125292471 12529247 Back disorder
125292471 12529247 Blood glucose increased
125292471 12529247 Colitis ulcerative
125292471 12529247 Diarrhoea
125292471 12529247 Fatigue
125292471 12529247 Headache

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found