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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125421601 | 12542160 | 1 | I | 20160622 | 20160708 | 20160708 | PER | US-009507513-1606USA012749 | MERCK | 0.00 | Y | 0.00000 | 20160708 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125421601 | 12542160 | 1 | PS | JANUVIA | SITAGLIPTIN PHOSPHATE | 1 | Oral | 100 MG, UNK | 21995 | 100 | MG | FILM-COATED TABLET | |||||||
| 125421601 | 12542160 | 2 | SS | JANUVIA | SITAGLIPTIN PHOSPHATE | 1 | Oral | CUTS MEDICATION IN TO LOWER DOSAGE AMOUNT TO 50MG TO EXPERIENCE LESS SIDE EFFECTS | 21995 | FILM-COATED TABLET |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125421601 | 12542160 | Adverse event | |
| 125421601 | 12542160 | Confusional state | |
| 125421601 | 12542160 | Intentional product misuse | |
| 125421601 | 12542160 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |