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
127102801 12710280 1 I 20160707 20160902 20160902 EXP US-UCBSA-2016025484 UCB 0.00 M Y 0.00000 20160902 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
127102801 12710280 1 PS LEVETIRACETAM. LEVETIRACETAM 1 HIGHEST DOSE 21035
127102801 12710280 2 SS LEVETIRACETAM. LEVETIRACETAM 1 UNK, 2X/DAY (BID) 21035 BID
127102801 12710280 3 SS LEVETIRACETAM. LEVETIRACETAM 1 1000 MG, 3X/DAY (TID) 21035 1000 MG TID
127102801 12710280 4 C LAMICTAL LAMOTRIGINE 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127102801 12710280 1 Product used for unknown indication
127102801 12710280 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127102801 12710280 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127102801 12710280 Depression
127102801 12710280 Headache
127102801 12710280 Memory impairment
127102801 12710280 Off label use
127102801 12710280 Petit mal epilepsy
127102801 12710280 Seizure
127102801 12710280 Tremor

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

no results found

Therapies reported

no results found