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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5578149 | 6517271 | I | 5578149-X | 20071219 | 20071231 | EXP | GB-PFIZER INC-2007108001 | PFIZER INC | 23 | YR | M | Y | 20071231 | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5578149 | 1009350714 | PS | CETIRIZINE HCL | 1 | 19835 | ||||||
| 5578149 | 1009350715 | SS | NEFOPAM | 2 | |||||||
| 5578149 | 1009350716 | SS | VENLAFAXINE HCL | 1 | |||||||
| 5578149 | 1009350717 | SS | CO-CODAMOL | 2 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5578149 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 5578149 | CONVULSION |
| 5578149 | FALL |
| 5578149 | OVERDOSE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |