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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5282291 | 6276612 | I | 5282291-0 | 20070320 | 20070331 | EXP | CA-PFIZER INC-2007023817 | PFIZER INC | Y | 20070330 | MD | CANADA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5282291 | 1008316857 | PS | LYRICA | 1 | ORAL | 21446 | |||||
5282291 | 1008316858 | I | DRUG, UNSPECIFIED | 2 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
5282291 | OT |
Reactions reported
Event ID | PT |
---|---|
5282291 | BLOOD PRESSURE DECREASED |
5282291 | DRUG INTERACTION |
5282291 | SYNCOPE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |