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
126465421 12646542 1 I 2016 20160805 20160812 20160812 EXP US-UCBSA-2016030638 UCB 0.00 A M Y 89.00000 KG 20160812 MD 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
126465421 12646542 1 PS KEPPRA LEVETIRACETAM 1 750 MG, 2X/DAY (BID) Y 21035 750 MG FILM-COATED TABLET BID
126465421 12646542 2 SS KEPPRA LEVETIRACETAM 1 500 MG, 2X/DAY (BID) Y 21035 500 MG FILM-COATED TABLET BID
126465421 12646542 3 C IBUPROFEN. IBUPROFEN 1 UNK U 0
126465421 12646542 4 C LORATADINE. LORATADINE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126465421 12646542 1 Product used for unknown indication
126465421 12646542 3 Product used for unknown indication
126465421 12646542 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126465421 12646542 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126465421 12646542 Agitation
126465421 12646542 Frustration tolerance decreased
126465421 12646542 Headache
126465421 12646542 Insomnia
126465421 12646542 Seizure
126465421 12646542 Stress at work

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
126465421 12646542 1 20160524 2016 0
126465421 12646542 2 2016 20160713 0
126465421 12646542 3 20160407 0
126465421 12646542 4 20160622 0