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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5282298 | 6276622 | I | 5282298-3 | 20070320 | 20070331 | EXP | US-PFIZER INC-2007023610 | PFIZER INC | M | Y | 20070330 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5282298 | 1008316885 | PS | NEURONTIN | 1 | 020235 | ||||||
5282298 | 1008316886 | SS | NEURONTIN | 1 | 020235 | ||||||
5282298 | 1008316887 | C | LORTAB | 1 | |||||||
5282298 | 1008316888 | C | MORPHINE | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5282298 | 1008316885 | BACK PAIN |
5282298 | 1008316886 | PAIN IN EXTREMITY |
Outcome of event
Event ID | OUTC COD |
---|---|
5282298 | OT |
Reactions reported
Event ID | PT |
---|---|
5282298 | EUPHORIC MOOD |
5282298 | IMPAIRED DRIVING ABILITY |
5282298 | OCULAR HYPERAEMIA |
5282298 | VISION BLURRED |
5282298 | VISUAL DISTURBANCE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |