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
127443272 12744327 2 F 201603 20160908 20160914 20160915 EXP MX-UCBSA-2016034943 UCB 73.35 YR M Y 72.00000 KG 20160915 CN MX MX

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
127443272 12744327 1 PS LEVETIRACETAM. LEVETIRACETAM 1 500 MG, 2X/DAY (BID) (500MG/12 HRS) U 21035 500 MG BID
127443272 12744327 2 SS LEVETIRACETAM. LEVETIRACETAM 1 Oral 1 G, 2X/DAY (BID) U 21035 1 G BID
127443272 12744327 3 C Acetylsalicylic acid ASPIRIN 1 ONCE DAILY (QD) (1 TABLET/24 HRS) U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127443272 12744327 1 Aphasia
127443272 12744327 2 Off label use
127443272 12744327 3 Cardiovascular disorder

Outcome of event

Event ID CASEID OUTC COD
127443272 12744327 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127443272 12744327 Chronic myeloid leukaemia
127443272 12744327 Off label use

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
127443272 12744327 1 201603 201603 0
127443272 12744327 2 20160324 0
127443272 12744327 3 201605 0