Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126473441 | 12647344 | 1 | I | 20160620 | 20160728 | 20160812 | 20160812 | EXP | IT-LUPIN PHARMACEUTICALS INC.-2016-03486 | LUPIN | 52.00 | YR | M | Y | 0.00000 | 20160812 | CN | IT | IT |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126473441 | 12647344 | 1 | PS | LEVETIRACETAM. | LEVETIRACETAM | 1 | Unknown | UNKNOWN | 78154 | ||||||||||
| 126473441 | 12647344 | 2 | SS | TEGRETOL | CARBAMAZEPINE | 1 | Unknown | 200 MG IN THE MORNING AND 400 MG IN THE EVENING | UNKNOWN | 0 | |||||||||
| 126473441 | 12647344 | 3 | SS | TEGRETOL | CARBAMAZEPINE | 1 | Unknown | 300 MG IN THE MORNING AND 400 MG IN THE EVENING | UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126473441 | 12647344 | 1 | Product used for unknown indication |
| 126473441 | 12647344 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126473441 | 12647344 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126473441 | 12647344 | Syncope | |
| 126473441 | 12647344 | Tremor |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |