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
121116293 12111629 3 F 20160603 20160224 20160818 EXP SE-ABBVIE-16P-150-1564460-00 ABBVIE 0.00 C F Y 0.00000 20160818 CN SE SE

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
121116293 12111629 1 PS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Unknown 51985 20725

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121116293 12111629 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
121116293 12111629 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121116293 12111629 Abdominal pain
121116293 12111629 Drug ineffective
121116293 12111629 Product taste abnormal
121116293 12111629 Steatorrhoea
121116293 12111629 Weight decreased

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

no results found

Therapies reported

no results found