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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127185631 | 12718563 | 1 | I | 20160813 | 20160829 | 20160906 | 20160906 | EXP | GB-ASTRAZENECA-2016SE92416 | ASTRAZENECA | 57.00 | YR | F | Y | 105.30000 | KG | 20160906 | OT | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127185631 | 12718563 | 1 | PS | BYETTA | EXENATIDE | 1 | Subcutaneous | 10 | UG | Y | U | 15K028 | 21773 | 5 | UG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | BID | ||
| 127185631 | 12718563 | 2 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | 0 | ||||||||||||
| 127185631 | 12718563 | 3 | C | CYCLIZINE | CYCLIZINE | 1 | 0 | ||||||||||||
| 127185631 | 12718563 | 4 | C | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | 0 | ||||||||||||
| 127185631 | 12718563 | 5 | C | LEVOTHYROXINE SODIUM. | LEVOTHYROXINE SODIUM | 1 | 0 | ||||||||||||
| 127185631 | 12718563 | 6 | C | LISINOPRIL. | LISINOPRIL | 1 | 0 | ||||||||||||
| 127185631 | 12718563 | 7 | C | NOVOMIX | INSULIN ASPART | 1 | 0 | ||||||||||||
| 127185631 | 12718563 | 8 | C | TRAMADOL. | TRAMADOL | 1 | 0 | ||||||||||||
| 127185631 | 12718563 | 9 | C | ZOMORPH | MORPHINE SULFATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127185631 | 12718563 | 1 | Type 2 diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127185631 | 12718563 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127185631 | 12718563 | Abdominal pain | |
| 127185631 | 12718563 | Anaphylactic reaction | |
| 127185631 | 12718563 | Throat irritation | |
| 127185631 | 12718563 | 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 |
|---|---|---|---|---|---|---|
| 127185631 | 12718563 | 1 | 20160812 | 20160815 | 0 |