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
126859361 12685936 1 I 20151111 20160628 20160825 20160825 EXP SE-ABBVIE-16P-150-1678882-00 ABBVIE 0.00 F Y 0.00000 20160825 OT 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
126859361 12685936 1 PS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Oral Y Y UNKNOWN 20725 25000 IU/KG TID
126859361 12685936 2 SS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Oral Y Y UNKNOWN 20725 25000 IU/KG TID
126859361 12685936 3 SS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Oral Y Y UNKNOWN 20725 50000 IU/KG TID
126859361 12685936 4 SS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Unknown TESTED CREON AGAIN FOR A FEW DAYS Y Y UNKNOWN 20725

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126859361 12685936 1 Biliopancreatic bypass
126859361 12685936 2 Duodenal switch

Outcome of event

Event ID CASEID OUTC COD
126859361 12685936 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126859361 12685936 Oedema peripheral Oedema peripheral
126859361 12685936 Periorbital oedema Periorbital oedema

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
126859361 12685936 1 20160616 20160627 0
126859361 12685936 2 20141003 0
126859361 12685936 4 20150630 0