Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040241 | 6075325 | I | 5040241-6 | 20060401 | 20060626 | 20060630 | EXP | US-JNJFOC-20060503079 | MCNEIL CONSUMER PRODUCTS USA REGULATORY REPORTING | M | Y | 20060630 | CN | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040241 | 1007430358 | PS | EXTRA STRENGTH TYLENOL | 1 | ORAL | MAA384 | |||||
| 5040241 | 1007430359 | C | METOPROLOL TARTRATE | 1 | |||||||
| 5040241 | 1007430360 | C | COUMADIN | 1 | |||||||
| 5040241 | 1007430361 | C | FUROSEMIDE | 1 | |||||||
| 5040241 | 1007430362 | C | ZOCOR | 1 | |||||||
| 5040241 | 1007430363 | C | VERAPAMIL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5040241 | 1007430358 | SLEEP DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5040241 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5040241 | SYNCOPE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |