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
125497441 12549744 1 I 20160705 20160712 20160712 EXP US-ABBVIE-16P-163-1669987-00 ABBVIE 0.00 F Y 0.00000 20160712 CN US US

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
125497441 12549744 1 PS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Unknown U UNKNOWN 20725

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125497441 12549744 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125497441 12549744 OT
125497441 12549744 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125497441 12549744 Amylase abnormal
125497441 12549744 Anxiety
125497441 12549744 Coronary artery occlusion
125497441 12549744 Depressed mood
125497441 12549744 Fall
125497441 12549744 Feeling guilty
125497441 12549744 Lipase abnormal
125497441 12549744 Myocardial infarction
125497441 12549744 Pain
125497441 12549744 Panic attack

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

no results found

Therapies reported

no results found