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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5282271 | 6276589 | I | 5282271-5 | 20070317 | 20070320 | 20070331 | EXP | DE-PFIZER INC-2007023259 | PFIZER INC | F | Y | 85 | KG | 20070330 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5282271 | 1008316790 | PS | LYRICA | 1 | ORAL | 021446 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5282271 | OT |
Reactions reported
Event ID | PT |
---|---|
5282271 | CARDIOVASCULAR INSUFFICIENCY |
5282271 | DISSOCIATION |
5282271 | DIZZINESS |
5282271 | DYSSTASIA |
5282271 | HYPOKINESIA |
5282271 | STARING |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5282271 | 1008316790 | 20070317 | 20070319 |