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
126544481 12654448 1 I 20160809 20160816 20160816 EXP DE-UCBSA-2016031214 UCB 74.00 YR F Y 0.00000 20160816 CN 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
126544481 12654448 1 PS Levetiracetam UCB LEVETIRACETAM 1 5000 MG DAILY U U 21035
126544481 12654448 2 SS Levetiracetam UCB LEVETIRACETAM 1 DOWN TITRATED FROM 5000 MG TO 2000 MG DAILY U U 21035
126544481 12654448 3 SS LEVETIRACETAM. LEVETIRACETAM 1 UNK U U 0
126544481 12654448 4 C LAMOTRIGINE. LAMOTRIGINE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126544481 12654448 1 Product used for unknown indication
126544481 12654448 3 Product used for unknown indication
126544481 12654448 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126544481 12654448 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126544481 12654448 Accidental overdose
126544481 12654448 Aggression
126544481 12654448 Delusion
126544481 12654448 Off label use
126544481 12654448 Withdrawal syndrome

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

no results found

Therapies reported

no results found