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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127966941 | 12796694 | 1 | I | 20160323 | 20160921 | 20160929 | 20160929 | EXP | CN-ELI_LILLY_AND_COMPANY-CN201609007852 | ELI LILLY AND CO | 53.00 | YR | F | Y | 0.00000 | 20160929 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127966941 | 12796694 | 1 | PS | HUMULIN 70/30 | INSULIN HUMAN | 1 | Subcutaneous | 10 IU, BID | U | U | C390983C | 18780 | 10 | IU | BID |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127966941 | 12796694 | 1 | Type 2 diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127966941 | 12796694 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127966941 | 12796694 | Blood glucose decreased | |
| 127966941 | 12796694 | Blood pressure decreased | |
| 127966941 | 12796694 | Dizziness | |
| 127966941 | 12796694 | Hyperhidrosis | |
| 127966941 | 12796694 | Muscular weakness | |
| 127966941 | 12796694 | Palpitations | |
| 127966941 | 12796694 | Tremor |
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 |
|---|---|---|---|---|---|---|
| 127966941 | 12796694 | 1 | 20160322 | 20160323 | 0 |