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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124217593 | 12421759 | 3 | F | 2016 | 20160712 | 20160531 | 20160726 | PER | US-009507513-1605USA001336 | MERCK | 77.68 | YR | F | Y | 77.10000 | KG | 20160726 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124217593 | 12421759 | 1 | PS | JANUMET | METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE | 1 | Oral | 1 TABLET (50/1000 MG), BID | Y | M000794 | 22044 | 1 | DF | FILM-COATED TABLET | BID | ||||
| 124217593 | 12421759 | 2 | SS | JANUMET | METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE | 1 | Oral | UNK, UNKNOWN | 22044 | FILM-COATED TABLET | |||||||||
| 124217593 | 12421759 | 3 | C | LOVASTATIN. | LOVASTATIN | 1 | U | 0 | |||||||||||
| 124217593 | 12421759 | 4 | C | LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM | 1 | Oral | 100/25 | 0 | TABLET | |||||||||
| 124217593 | 12421759 | 5 | C | ZOCOR | SIMVASTATIN | 1 | Oral | 20MG, UNK | U | 0 | 20 | MG | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124217593 | 12421759 | 1 | Type 2 diabetes mellitus |
| 124217593 | 12421759 | 2 | Type 2 diabetes mellitus |
| 124217593 | 12421759 | 3 | Blood pressure measurement |
| 124217593 | 12421759 | 4 | Hypertension |
| 124217593 | 12421759 | 5 | Blood cholesterol |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124217593 | 12421759 | Blood glucose increased | |
| 124217593 | 12421759 | Diarrhoea | |
| 124217593 | 12421759 | Dyspepsia | |
| 124217593 | 12421759 | Headache | |
| 124217593 | 12421759 | Product quality issue | |
| 124217593 | 12421759 | Tongue discomfort |
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 |
|---|---|---|---|---|---|---|
| 124217593 | 12421759 | 1 | 20160415 | 20160416 | 0 |