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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7487805 | 7912774 | F | 7487805-8 | 20110504 | 20110518 | EXP | US-JNJFOC-20110407778 | ORTHO-MCNEIL-JANSSEN PHARMACEUTICALS, INC. | YR | Y | 20110518 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7487805 | 1016527261 | SS | LYRICA | 1 | UNKNOWN | ||||||
7487805 | 1016527260 | PS | ULTRAM | 1 | UNKNOWN | 020281 | |||||
7487805 | 1016527262 | SS | GABAPENTIN | 1 | UNKNOWN | ||||||
7487805 | 1016527263 | SS | DEPAKOTE | 1 | UNKNOWN |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7487805 | 1016527261 | PRODUCT USED FOR UNKNOWN INDICATION |
7487805 | 1016527260 | PRODUCT USED FOR UNKNOWN INDICATION |
7487805 | 1016527262 | PRODUCT USED FOR UNKNOWN INDICATION |
7487805 | 1016527263 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
7487805 | OT |
Reactions reported
Event ID | PT |
---|---|
7487805 | NEUROPATHY PERIPHERAL |
7487805 | CONVULSIVE THRESHOLD LOWERED |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |