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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125438641 | 12543864 | 1 | I | 20160629 | 20160711 | 20160711 | EXP | US-WEST-WARD PHARMACEUTICALS CORP.-US-H14001-16-01244 | WESTWARD | EILERS B,ALBERS E,LAW Y,MIKE MCMULLAN D,SHAW D,KEMNA M. POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME AFTER PEDIATRIC HEART TRANSPLANTATION: INCREASED RISK FOR CHILDREN WITH PREEXISTING GLENN/FONTAN PHYSIOLOGY. PEDIATRIC TRANSPLANTATION 2016;20(4):552-558. | 19.00 | YR | F | Y | 0.00000 | 20160708 | MD | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125438641 | 12543864 | 1 | PS | LEVETIRACETAM. | LEVETIRACETAM | 1 | Unknown | 78582 | |||||||||||
| 125438641 | 12543864 | 2 | SS | PHENYTOIN. | PHENYTOIN | 1 | Unknown | 84307 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125438641 | 12543864 | 1 | Product used for unknown indication |
| 125438641 | 12543864 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125438641 | 12543864 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125438641 | 12543864 | Posterior reversible encephalopathy syndrome |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |