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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126580001 | 12658000 | 1 | I | 20160722 | 20160808 | 20160816 | 20160816 | EXP | IE-SA-2016SA145512 | AVENTIS | 39.00 | YR | A | F | Y | 0.00000 | 20160816 | MD | IE | IE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126580001 | 12658000 | 1 | PS | LANTUS | INSULIN GLARGINE | 1 | Subcutaneous | UNK | 21081 | 22 | IU | SOLUTION FOR INJECTION | QD | ||||||
| 126580001 | 12658000 | 2 | SS | LANTUS | INSULIN GLARGINE | 1 | Subcutaneous | DOSE:24 UNIT(S) | UNK | 21081 | SOLUTION FOR INJECTION | QD | |||||||
| 126580001 | 12658000 | 3 | SS | LANTUS | INSULIN GLARGINE | 1 | Subcutaneous | UNK | 21081 | 22 | IU | SOLUTION FOR INJECTION | QD | ||||||
| 126580001 | 12658000 | 4 | SS | APIDRA | INSULIN GLULISINE | 1 | Subcutaneous | DOSE - 1:7, 1:9, 1:9 | Y | UNK | 21629 | SOLUTION FOR INJECTION | |||||||
| 126580001 | 12658000 | 5 | SS | APIDRA | INSULIN GLULISINE | 1 | Subcutaneous | DOSE - 1:9, 1:9, 1:9 | Y | UNK | 21629 | SOLUTION FOR INJECTION | |||||||
| 126580001 | 12658000 | 6 | SS | APIDRA | INSULIN GLULISINE | 1 | Subcutaneous | DOSE - 1:10, 1:10, 1:10 | Y | UNK | 21629 | SOLUTION FOR INJECTION | |||||||
| 126580001 | 12658000 | 7 | C | FOLIC ACID. | FOLIC ACID | 1 | Unknown | 0 | |||||||||||
| 126580001 | 12658000 | 8 | C | LABETALOL | LABETALOLLABETALOL HYDROCHLORIDE | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126580001 | 12658000 | 1 | Type 1 diabetes mellitus |
| 126580001 | 12658000 | 2 | Type 1 diabetes mellitus |
| 126580001 | 12658000 | 3 | Type 1 diabetes mellitus |
| 126580001 | 12658000 | 4 | Type 1 diabetes mellitus |
| 126580001 | 12658000 | 5 | Type 1 diabetes mellitus |
| 126580001 | 12658000 | 6 | Type 1 diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126580001 | 12658000 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126580001 | 12658000 | Exposure during pregnancy | |
| 126580001 | 12658000 | Hypoglycaemia | |
| 126580001 | 12658000 | 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 |
|---|---|---|---|---|---|---|
| 126580001 | 12658000 | 1 | 200610 | 0 | ||
| 126580001 | 12658000 | 2 | 20140708 | 0 | ||
| 126580001 | 12658000 | 4 | 200610 | 201607 | 0 | |
| 126580001 | 12658000 | 5 | 20160722 | 0 | ||
| 126580001 | 12658000 | 7 | 201603 | 0 | ||
| 126580001 | 12658000 | 8 | 20160624 | 0 |