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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 101627321 | 10162732 | 1 | I | 201206 | 20140502 | 20140509 | 20140509 | EXP | DK-PFIZER INC-2014126769 | PFIZER | 82.00 | YR | F | Y | 0.00000 | 20140509 | N | LW | DK | DK |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 101627321 | 10162732 | 1 | PS | Cordarone | 1 | UNKNOWN | UNK | D | 18972 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 101627321 | 10162732 | 1 | Atrial fibrillation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 101627321 | 10162732 | HO |
| 101627321 | 10162732 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 101627321 | 10162732 | Cardiac failure chronic | |
| 101627321 | 10162732 | Cough | |
| 101627321 | 10162732 | Dyspnoea | |
| 101627321 | 10162732 | Fatigue | |
| 101627321 | 10162732 | Lung disorder | |
| 101627321 | 10162732 | Pulmonary fibrosis |
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 |
|---|---|---|---|---|---|---|
| 101627321 | 10162732 | 1 | 200011 | 201208 | 0 |