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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126209092 | 12620909 | 2 | F | 201505 | 20160729 | 20160804 | 20160812 | EXP | IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-121422 | RANBAXY | 18.00 | YR | M | Y | 0.00000 | 20160812 | OT | GB | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126209092 | 12620909 | 1 | PS | LEVETIRACETAM. | LEVETIRACETAM | 1 | Unknown | 250 MG, BID | Y | 203059 | 250 | MG | Q12H | ||||||
| 126209092 | 12620909 | 2 | SS | LEVETIRACETAM. | LEVETIRACETAM | 1 | Unknown | 500 MG, BID | Y | 203059 | 500 | MG | Q12H |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126209092 | 12620909 | 1 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126209092 | 12620909 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126209092 | 12620909 | Paradoxical drug reaction | |
| 126209092 | 12620909 | Seizure |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |