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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127759193 | 12775919 | 3 | F | 201609 | 20160920 | 20160923 | 20160927 | EXP | PHHY2016IT128858 | SANDOZ | 83.24 | YR | F | Y | 0.00000 | 20160927 | OT | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127759193 | 12775919 | 1 | PS | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | Y | 70268 | TABLET | |||||||||
| 127759193 | 12775919 | 2 | C | VERTISERC | BETAHISTINE HYDROCHLORIDE | 1 | Oral | U | 0 | TABLET | |||||||||
| 127759193 | 12775919 | 3 | C | PERIDON | DOMPERIDONE | 1 | Oral | U | 0 | FILM-COATED TABLET | |||||||||
| 127759193 | 12775919 | 4 | C | LASIX | FUROSEMIDE | 1 | Unknown | 1 UNK, UNK | Y | 0 | 1 | DF | |||||||
| 127759193 | 12775919 | 5 | C | LASIX | FUROSEMIDE | 1 | Unknown | 0.5 DF, UNK | Y | 0 | .5 | DF | |||||||
| 127759193 | 12775919 | 6 | C | TICLOPIDINE | TICLOPIDINE | 1 | Oral | U | 0 | TABLET | |||||||||
| 127759193 | 12775919 | 7 | C | ZYRTEC | CETIRIZINE HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
| 127759193 | 12775919 | 8 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | Oral | U | 0 | GASTRO-RESISTANT TABLET | |||||||||
| 127759193 | 12775919 | 9 | C | ENALAPRIL | ENALAPRIL | 1 | Oral | U | 0 | TABLET | |||||||||
| 127759193 | 12775919 | 10 | C | CALCIUM CARBONATE. | CALCIUM CARBONATE | 1 | Oral | U | 0 | TABLET | |||||||||
| 127759193 | 12775919 | 11 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Oral | U | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127759193 | 12775919 | 1 | Hyperuricaemia |
| 127759193 | 12775919 | 2 | Product used for unknown indication |
| 127759193 | 12775919 | 3 | Product used for unknown indication |
| 127759193 | 12775919 | 4 | Product used for unknown indication |
| 127759193 | 12775919 | 6 | Product used for unknown indication |
| 127759193 | 12775919 | 7 | Product used for unknown indication |
| 127759193 | 12775919 | 8 | Product used for unknown indication |
| 127759193 | 12775919 | 9 | Product used for unknown indication |
| 127759193 | 12775919 | 10 | Product used for unknown indication |
| 127759193 | 12775919 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127759193 | 12775919 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127759193 | 12775919 | Nausea | |
| 127759193 | 12775919 | Oedema peripheral | |
| 127759193 | 12775919 | Pruritus | |
| 127759193 | 12775919 | Toxic skin eruption | |
| 127759193 | 12775919 | Vertigo |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |