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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126556152 | 12655615 | 2 | F | 20160627 | 20160811 | 20160816 | 20160818 | EXP | PHHY2016IT110719 | SANDOZ | 78.74 | YR | F | Y | 0.00000 | 20160818 | OT | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126556152 | 12655615 | 1 | PS | METFORMINE HCL | METFORMIN HYDROCHLORIDE | 1 | Oral | 1500 MG, QD | U | 75985 | 1500 | MG | TABLET | QD | |||||
| 126556152 | 12655615 | 2 | SS | DIAMICRON | GLICLAZIDE | 1 | Oral | 30 MG, QD | U | 0 | 30 | MG | MODIFIED RELEASE TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126556152 | 12655615 | 1 | Diabetes mellitus |
| 126556152 | 12655615 | 2 | Diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126556152 | 12655615 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126556152 | 12655615 | Hyperhidrosis | |
| 126556152 | 12655615 | Hypoglycaemia | |
| 126556152 | 12655615 | Hypokinesia | |
| 126556152 | 12655615 | Pallor |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |