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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125982412 | 12598241 | 2 | F | 20160808 | 20160726 | 20160816 | EXP | PHHY2016BR100964 | NOVARTIS | 0.00 | M | Y | 90.00000 | KG | 20160816 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125982412 | 12598241 | 1 | SS | GALVUS MET | METFORMIN HYDROCHLORIDEVILDAGLIPTIN | 1 | Oral | 1 DF, BID | 0 | 1 | DF | TABLET | BID | ||||||
| 125982412 | 12598241 | 2 | SS | GALVUS MET | METFORMIN HYDROCHLORIDEVILDAGLIPTIN | 1 | Oral | 2 DF (850MG OF METFORMIN/50MG OF VILDAGLIPTIN), QD | 0 | 2 | DF | TABLET | QD | ||||||
| 125982412 | 12598241 | 3 | PS | DIOVAN | VALSARTAN | 1 | Oral | 160 MG, QD | 1520355 | 21283 | 160 | MG | TABLET | QD | |||||
| 125982412 | 12598241 | 4 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 20 MG, QD | SM8976 | 0 | 20 | MG | TABLET | QD | |||||
| 125982412 | 12598241 | 5 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | Oral | 75 MG, QD | 0 | 75 | MG | QD | |||||||
| 125982412 | 12598241 | 6 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Oral | 20 MG, QD | 0 | 20 | MG | QD | |||||||
| 125982412 | 12598241 | 7 | C | INSULIN GLARGINE | INSULIN GLARGINE | 1 | Subcutaneous | 20 UNITS IN THE MORNING, 20 UNITS AT NIGHT | 0 | ||||||||||
| 125982412 | 12598241 | 8 | C | REGULAR INSULIN | INSULIN NOS | 1 | Unknown | UNK UNK, PRN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125982412 | 12598241 | 1 | Product used for unknown indication |
| 125982412 | 12598241 | 3 | Product used for unknown indication |
| 125982412 | 12598241 | 4 | Product used for unknown indication |
| 125982412 | 12598241 | 5 | Product used for unknown indication |
| 125982412 | 12598241 | 6 | Product used for unknown indication |
| 125982412 | 12598241 | 7 | Diabetes mellitus |
| 125982412 | 12598241 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125982412 | 12598241 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125982412 | 12598241 | Bronchitis | |
| 125982412 | 12598241 | Cerebrovascular accident | |
| 125982412 | 12598241 | Cough | |
| 125982412 | 12598241 | Hypoaesthesia | |
| 125982412 | 12598241 | Hypoaesthesia oral | |
| 125982412 | 12598241 | Malaise | |
| 125982412 | 12598241 | Memory impairment | |
| 125982412 | 12598241 | Muscular weakness | |
| 125982412 | 12598241 | Myocardial infarction | |
| 125982412 | 12598241 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |