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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124904013 | 12490401 | 3 | F | 201605 | 20160628 | 20160622 | 20160706 | EXP | CN-ASTRAZENECA-2016SE57648 | ASTRAZENECA | 54.00 | YR | F | Y | 0.00000 | 20160706 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124904013 | 12490401 | 1 | PS | BYETTA | EXENATIDE | 1 | Subcutaneous | 320 | UG | Y | U | 21773 | 5 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID | |||
124904013 | 12490401 | 2 | SS | BYETTA | EXENATIDE | 1 | Subcutaneous | 320 | UG | Y | U | 21773 | 5 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID | |||
124904013 | 12490401 | 3 | SS | BYETTA | EXENATIDE | 1 | Subcutaneous | 320 | UG | Y | U | 21773 | 10 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID | |||
124904013 | 12490401 | 4 | SS | BYETTA | EXENATIDE | 1 | Subcutaneous | 320 | UG | Y | U | 21773 | 10 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID | |||
124904013 | 12490401 | 5 | C | ANTIHYPERTENSIVE DRUGS | UNSPECIFIED INGREDIENT | 1 | DAILY | 0 | |||||||||||
124904013 | 12490401 | 6 | C | DIABETES DRUGS | UNSPECIFIED INGREDIENT | 1 | DAILY | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124904013 | 12490401 | 1 | Diabetes mellitus |
124904013 | 12490401 | 2 | Blood glucose increased |
124904013 | 12490401 | 3 | Diabetes mellitus |
124904013 | 12490401 | 4 | Blood glucose increased |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124904013 | 12490401 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124904013 | 12490401 | Asthenia | |
124904013 | 12490401 | Blood glucose decreased | |
124904013 | 12490401 | Blood pressure increased | |
124904013 | 12490401 | Dizziness | |
124904013 | 12490401 | Hypoacusis | |
124904013 | 12490401 | Syncope | |
124904013 | 12490401 | 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 |
---|---|---|---|---|---|---|
124904013 | 12490401 | 1 | 20160418 | 20160517 | 0 | |
124904013 | 12490401 | 2 | 20160418 | 20160517 | 0 | |
124904013 | 12490401 | 3 | 20160518 | 201605 | 0 | |
124904013 | 12490401 | 4 | 20160518 | 201605 | 0 |