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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126699592 | 12669959 | 2 | F | 20150629 | 20160623 | 20160820 | 20160909 | EXP | CN-ASTRAZENECA-2016SE60856 | ASTRAZENECA | 29.00 | YR | F | Y | 41.00000 | KG | 20160909 | CN | CN | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126699592 | 12669959 | 1 | PS | BYETTA | EXENATIDE | 1 | Subcutaneous | U | U | 21773 | 10 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID | |||||
126699592 | 12669959 | 2 | SS | BYETTA | EXENATIDE | 1 | Subcutaneous | U | U | 21773 | 5 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID | |||||
126699592 | 12669959 | 3 | SS | BYETTA | EXENATIDE | 1 | Subcutaneous | U | U | 21773 | 10 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID | |||||
126699592 | 12669959 | 4 | SS | BYETTA | EXENATIDE | 1 | Subcutaneous | U | U | 21773 | 10 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID | |||||
126699592 | 12669959 | 5 | SS | BYETTA | EXENATIDE | 1 | Subcutaneous | U | U | 21773 | 10 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126699592 | 12669959 | 1 | Diabetes mellitus |
126699592 | 12669959 | 2 | Diabetes mellitus |
126699592 | 12669959 | 3 | Diabetes mellitus |
126699592 | 12669959 | 4 | Diabetes mellitus |
126699592 | 12669959 | 5 | Diabetes mellitus |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126699592 | 12669959 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126699592 | 12669959 | Abdominal discomfort | |
126699592 | 12669959 | Abdominal pain upper | |
126699592 | 12669959 | Blood glucose fluctuation | |
126699592 | 12669959 | Chronic gastritis | |
126699592 | 12669959 | Constipation | |
126699592 | 12669959 | Dizziness | |
126699592 | 12669959 | Drug ineffective | |
126699592 | 12669959 | Dyspepsia | |
126699592 | 12669959 | Eructation | |
126699592 | 12669959 | Gastrooesophageal reflux disease | |
126699592 | 12669959 | Generalised erythema | |
126699592 | 12669959 | Headache | |
126699592 | 12669959 | Hypoglycaemia | |
126699592 | 12669959 | Intentional product misuse | |
126699592 | 12669959 | Nausea | |
126699592 | 12669959 | Night sweats | |
126699592 | 12669959 | Palpitations | |
126699592 | 12669959 | Somnolence | |
126699592 | 12669959 | Vomiting |
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 |
---|---|---|---|---|---|---|
126699592 | 12669959 | 1 | 2013 | 0 | ||
126699592 | 12669959 | 2 | 20150629 | 0 | ||
126699592 | 12669959 | 3 | 201505 | 0 | ||
126699592 | 12669959 | 4 | 201504 | 0 | ||
126699592 | 12669959 | 5 | 20150730 | 0 |