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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126198121 | 12619812 | 1 | I | 20150823 | 20160726 | 20160803 | 20160803 | EXP | CH-SWISSMEDIC-2016-06159 | CH-FRI-1000086637 | FOREST | 61.75 | YR | F | Y | 0.00000 | 20160803 | OT | DK | CH |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126198121 | 12619812 | 1 | PS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Oral | 21365 | 15 | GTT | ORAL DROPS | ||||||||
| 126198121 | 12619812 | 2 | SS | MARCUMAR | PHENPROCOUMON | 1 | Oral | 3 MG | U | 0 | 3 | MG | QD | ||||||
| 126198121 | 12619812 | 3 | C | BILOL/BISOPROLOL FUMARATE | BISOPROLOL FUMARATE | 1 | Oral | 0 | 5 | MG | |||||||||
| 126198121 | 12619812 | 4 | C | Bioflorin/Enterococcus faecalis | 2 | Unknown | 0 | CAPSULE | |||||||||||
| 126198121 | 12619812 | 5 | C | Amlodipin actavis/Amlodipine besilate | 2 | Unknown | 0 | 5 | MG | ||||||||||
| 126198121 | 12619812 | 6 | C | Imodium akut/Loperamide hydrochlorid | 2 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126198121 | 12619812 | 1 | Depression |
| 126198121 | 12619812 | 2 | Atrial fibrillation |
| 126198121 | 12619812 | 3 | Product used for unknown indication |
| 126198121 | 12619812 | 4 | Product used for unknown indication |
| 126198121 | 12619812 | 5 | Product used for unknown indication |
| 126198121 | 12619812 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126198121 | 12619812 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126198121 | 12619812 | Duodenal ulcer | |
| 126198121 | 12619812 | Haematemesis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |