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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126220351 | 12622035 | 1 | I | 2015 | 20160729 | 20160804 | 20160804 | EXP | US-PFIZER INC-2016369340 | PFIZER | 0.00 | F | Y | 0.00000 | 20160804 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126220351 | 12622035 | 1 | PS | DILANTIN | PHENYTOIN | 1 | UNK | U | 10151 | ||||||||||
126220351 | 12622035 | 2 | SS | KEPPRA | LEVETIRACETAM | 1 | 1000 MG, DAILY | U | 0 | 1000 | MG | ||||||||
126220351 | 12622035 | 3 | SS | LAMICTAL | LAMOTRIGINE | 1 | UNK, DAILY | U | 0 | ||||||||||
126220351 | 12622035 | 4 | SS | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | UNK | U | 0 | ||||||||||
126220351 | 12622035 | 5 | SS | KLONOPIN | CLONAZEPAM | 1 | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126220351 | 12622035 | 1 | Generalised tonic-clonic seizure |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126220351 | 12622035 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126220351 | 12622035 | Coma | |
126220351 | 12622035 | Drug ineffective | |
126220351 | 12622035 | Head injury | |
126220351 | 12622035 | Pain | |
126220351 | 12622035 | Road traffic accident | |
126220351 | 12622035 | Seizure |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |