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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126308311 | 12630831 | 1 | I | 20160802 | 20160808 | 20160808 | PER | GXBR2016US002484 | SANDOZ | 0.00 | F | Y | 80.38000 | KG | 20160808 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126308311 | 12630831 | 1 | PS | FUROSEMIDE TABLETS USP | FUROSEMIDE | 1 | Unknown | 20 MG, UNK | N | U | 18569 | 20 | MG | TABLET | |||||
| 126308311 | 12630831 | 2 | SS | FUROSEMIDE TABLETS USP | FUROSEMIDE | 1 | N | U | 18569 | TABLET | |||||||||
| 126308311 | 12630831 | 3 | SS | LATANOPROST. | LATANOPROST | 1 | Ophthalmic | UNK DF, QD | U | U | 0 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126308311 | 12630831 | 1 | Joint swelling |
| 126308311 | 12630831 | 2 | Peripheral swelling |
| 126308311 | 12630831 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126308311 | 12630831 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126308311 | 12630831 | Arthralgia | |
| 126308311 | 12630831 | Dyspnoea | |
| 126308311 | 12630831 | Eye disorder | |
| 126308311 | 12630831 | Heart rate increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |