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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126738801 | 12673880 | 1 | I | 20160817 | 20160822 | 20160822 | EXP | US-009507513-1608USA009291 | MERCK | 91.00 | YR | F | Y | 0.00000 | 20160822 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126738801 | 12673880 | 1 | PS | JANUVIA | SITAGLIPTIN PHOSPHATE | 1 | Oral | UNK | 21995 | FILM-COATED TABLET | |||||||||
| 126738801 | 12673880 | 2 | SS | JANUVIA | SITAGLIPTIN PHOSPHATE | 1 | Oral | UNK | 21995 | FILM-COATED TABLET |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126738801 | 12673880 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126738801 | 12673880 | Arthralgia | |
| 126738801 | 12673880 | Hyperkeratosis | |
| 126738801 | 12673880 | Pain in extremity | |
| 126738801 | 12673880 | Peripheral swelling | |
| 126738801 | 12673880 | Rash | |
| 126738801 | 12673880 | Skin exfoliation | |
| 126738801 | 12673880 | Swelling face |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |