The Safety Rates Drug Report

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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
122311032 12231103 2 F 20160803 20160401 20160810 EXP DE-UCBSA-2016011315 UCB 0.00 F Y 0.00000 20160810 MD DE DE

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
122311032 12231103 1 PS LEVETIRACETAM. LEVETIRACETAM 1 Intravenous (not otherwise specified) 4000 MG, UNK U U 21035 4000 MG
122311032 12231103 2 SS LEVETIRACETAM. LEVETIRACETAM 1 U U 21035
122311032 12231103 3 SS LEVETIRACETAM. LEVETIRACETAM 1 U U 21035
122311032 12231103 4 C VALPROATE VALPROIC ACID 1 1750 MG, UNK U 0 1750 MG
122311032 12231103 5 C TOPIRAMATE. TOPIRAMATE 1 UNK U 0
122311032 12231103 6 C Perampanel PERAMPANEL 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122311032 12231103 1 Status epilepticus
122311032 12231103 2 Epilepsy
122311032 12231103 3 Off label use
122311032 12231103 4 Product used for unknown indication
122311032 12231103 5 Product used for unknown indication
122311032 12231103 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122311032 12231103 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122311032 12231103 Drug ineffective
122311032 12231103 Off label use
122311032 12231103 Overdose

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

no results found

Therapies reported

no results found