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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7718870 | 8118196 | I | 7718870-8 | 20100513 | 20100616 | 20110817 | PER | 20108933 | MEDTRONIC, INC. | 20 | YR | F | N | 20100624 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7718870 | 1017421464 | PS | LIORESAL | 1 | INTRATHECAL | 130 MCG, DAILY, INTRATHECAL | D | D | 020075 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7718870 | 1017421464 | MUSCLE SPASTICITY |
Outcome of event
Event ID | OUTC COD |
---|---|
7718870 | OT |
Reactions reported
Event ID | PT |
---|---|
7718870 | HYPERTONIA |
7718870 | PRURITUS |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
7718870 | HP |
7718870 | CR |
Therapies reported
no results found |