The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
126416271 12641627 1 I 2009 20160803 20160810 20160810 EXP US-UCBSA-2016029892 UCB 0.00 F Y 0.00000 20160810 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
126416271 12641627 1 PS VIMPAT LACOSAMIDE 1 Oral 100 MG, 3X/DAY (TID) 22253 100 MG TID
126416271 12641627 2 SS KEPPRA LEVETIRACETAM 1 Oral UNK 0 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126416271 12641627 1 Epilepsy
126416271 12641627 2 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
126416271 12641627 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126416271 12641627 Complex partial seizures
126416271 12641627 Drug dispensing error
126416271 12641627 Fall
126416271 12641627 Generalised tonic-clonic seizure
126416271 12641627 Inappropriate schedule of drug administration
126416271 12641627 Rib fracture
126416271 12641627 Simple partial seizures

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126416271 12641627 1 200911 0
126416271 12641627 2 200911 0