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
101893036 10189303 6 F 2010 20160701 20140522 20160706 EXP US-ABBVIE-14P-163-1237897-00 ABBVIE 0.00 F Y 0.00000 20160706 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
101893036 10189303 1 PS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Unknown U UNKNOWN 20725

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101893036 10189303 1 Pancreatic insufficiency

Outcome of event

Event ID CASEID OUTC COD
101893036 10189303 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101893036 10189303 Abdominal distension
101893036 10189303 Abdominal pain upper
101893036 10189303 Benign pancreatic neoplasm
101893036 10189303 Diarrhoea
101893036 10189303 Dyspepsia
101893036 10189303 Fatigue
101893036 10189303 Infection
101893036 10189303 Malnutrition
101893036 10189303 Ovarian cancer
101893036 10189303 Pain
101893036 10189303 Pancreatitis
101893036 10189303 Pseudocyst
101893036 10189303 Vitamin D decreased
101893036 10189303 Weight decreased

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

no results found

Therapies reported

no results found