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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5282280 | 6276600 | I | 5282280-6 | 20070320 | 20070331 | EXP | DE-PFIZER INC-2007023382 | PFIZER INC | M | Y | 20070330 | MD | GERMANY |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5282280 | 1008316808 | PS | LYRICA | 1 | ORAL | DAILY DOSE:900MG | 021446 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5282280 | HO |
5282280 | OT |
Reactions reported
Event ID | PT |
---|---|
5282280 | CARDIAC FAILURE |
5282280 | OEDEMA |
5282280 | OVERDOSE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |