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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125209691 | 12520969 | 1 | I | 20160621 | 20160701 | 20160701 | EXP | BR-ELI_LILLY_AND_COMPANY-BR201606007797 | ELI LILLY AND CO | 0.00 | F | Y | 90.00000 | KG | 20160701 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125209691 | 12520969 | 1 | PS | HUMULIN N | INSULIN HUMAN | 1 | Subcutaneous | 18 IU, EACH MORNING | U | 18780 | 18 | IU | INJECTION | QD | |||||
| 125209691 | 12520969 | 2 | SS | HUMULIN N | INSULIN HUMAN | 1 | Subcutaneous | 32 IU, QD | U | 18780 | 32 | IU | INJECTION | QD | |||||
| 125209691 | 12520969 | 3 | SS | HUMULIN N | INSULIN HUMAN | 1 | Subcutaneous | 30 IU, EACH EVENING | U | 18780 | 30 | IU | INJECTION | QD | |||||
| 125209691 | 12520969 | 4 | SS | HUMULIN R | INSULIN HUMAN | 1 | Subcutaneous | 18 IU, EACH MORNING | U | 0 | 18 | IU | INJECTION | QD | |||||
| 125209691 | 12520969 | 5 | SS | HUMULIN R | INSULIN HUMAN | 1 | Subcutaneous | 18 IU, QD | U | 0 | 18 | IU | INJECTION | QD | |||||
| 125209691 | 12520969 | 6 | SS | HUMULIN R | INSULIN HUMAN | 1 | Subcutaneous | 10 IU, EACH EVENING | U | 0 | 10 | IU | INJECTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125209691 | 12520969 | 1 | Diabetes mellitus |
| 125209691 | 12520969 | 4 | Diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125209691 | 12520969 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125209691 | 12520969 | Cervix dystocia | |
| 125209691 | 12520969 | Exposure during breast feeding | |
| 125209691 | 12520969 | Exposure during pregnancy | |
| 125209691 | 12520969 | Injection site mass |
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 |
|---|---|---|---|---|---|---|
| 125209691 | 12520969 | 1 | 2005 | 0 | ||
| 125209691 | 12520969 | 2 | 2005 | 0 | ||
| 125209691 | 12520969 | 3 | 2005 | 0 | ||
| 125209691 | 12520969 | 4 | 2005 | 0 | ||
| 125209691 | 12520969 | 5 | 2005 | 0 | ||
| 125209691 | 12520969 | 6 | 2005 | 0 |