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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040242 | 6075326 | I | 5040242-8 | 20060627 | 20060630 | EXP | NO-JNJFOC-20060605884 | MCNEIL CONSUMER PRODUCTS USA REGULATORY REPORTING | F | Y | 20060630 | CN | NORWAY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040242 | 1007430364 | PS | PARACETAMOL | 2 | 19872 | ||||||
| 5040242 | 1007430365 | SS | PARACETAMOL | 2 | 019872 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5040242 | 1007430365 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5040242 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 5040242 | OVERDOSE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |