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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6082624 | 6912718 | I | 6082624-1 | 20090211 | 20090218 | EXP | US-PFIZER INC-2009168332 | PFIZERINC | M | Y | 20090218 | OT | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6082624 | 1011145441 | PS | MEDROL | 1 | 011153 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6082624 | OT |
Reactions reported
Event ID | PT |
---|---|
6082624 | APHONIA |
6082624 | HEART RATE INCREASED |
6082624 | HYPERSENSITIVITY |
6082624 | OBSTRUCTIVE AIRWAYS DISORDER |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |