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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126000012 | 12600001 | 2 | F | 20160215 | 20160722 | 20160727 | 20160803 | EXP | FR-PFIZER INC-2016356838 | PFIZER | 80.00 | YR | F | Y | 0.00000 | 20160803 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126000012 | 12600001 | 1 | PS | CORDARONE | AMIODARONE HYDROCHLORIDE | 1 | Oral | 200 MG, DAILY | 18972 | 200 | MG | TABLET | |||||||
| 126000012 | 12600001 | 2 | SS | DICLOFENAC | DICLOFENAC | 1 | Oral | UNK | U | 0 | |||||||||
| 126000012 | 12600001 | 3 | SS | KARDEGIC | ASPIRIN LYSINE | 1 | Oral | 75 MG, DAILY | Y | 0 | 75 | MG | POWDER FOR ORAL SOLUTION | ||||||
| 126000012 | 12600001 | 4 | SS | PREVISCAN | FLUINDIONE | 1 | Oral | 0.75 DF, DAILY | Y | 0 | .75 | DF | TABLET | ||||||
| 126000012 | 12600001 | 5 | SS | COLCHICINE. | COLCHICINE | 1 | Unknown | UNK | Y | 0 | |||||||||
| 126000012 | 12600001 | 6 | C | TEMERIT | NEBIVOLOL | 1 | 5 MG, DAILY | 0 | 5 | MG | |||||||||
| 126000012 | 12600001 | 7 | C | TEMESTA | LORAZEPAM | 1 | 2 MG, DAILY | 0 | 2 | MG | |||||||||
| 126000012 | 12600001 | 8 | C | IRBESARTAN. | IRBESARTAN | 1 | UNK, DAILY | 0 | |||||||||||
| 126000012 | 12600001 | 9 | C | ESOMEPRAZOLE | ESOMEPRAZOLE | 1 | UNK, DAILY | 0 | |||||||||||
| 126000012 | 12600001 | 10 | C | ATARAX | HYDROXYZINEHYDROXYZINE HYDROCHLORIDE | 1 | 100 MG, DAILY | 0 | 100 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126000012 | 12600001 | 1 | Atrial fibrillation |
| 126000012 | 12600001 | 4 | Prophylaxis |
| 126000012 | 12600001 | 5 | Gout |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126000012 | 12600001 | OT |
| 126000012 | 12600001 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126000012 | 12600001 | Anaemia | |
| 126000012 | 12600001 | Fall | |
| 126000012 | 12600001 | International normalised ratio increased | |
| 126000012 | 12600001 | Subcutaneous haematoma |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126000012 | 12600001 | 3 | 201602 | 0 |