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
114497233 11449723 3 F 201411 20160915 20150903 20160923 EXP AU-UCBSA-2015027442 UCB 59.00 YR F Y 0.00000 20160923 OT AU AU

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
114497233 11449723 1 PS KEPPRA LEVETIRACETAM 1 UNK UNK, 4X/DAY (QID) U U 21035 QID
114497233 11449723 2 SS Teriflunomide TERIFLUNOMIDE 1 Oral UNK U 0
114497233 11449723 3 C Thyroxin LEVOTHYROXINE 1 UNK U 0
114497233 11449723 4 C BACLOFEN. BACLOFEN 1 U 0
114497233 11449723 5 C Codeine phosphate CODEINE PHOSPHATE 1 UNK U 0
114497233 11449723 6 C SERC BETAHISTINE HYDROCHLORIDE 1 UNK U 0
114497233 11449723 7 C Paracetamol ACETAMINOPHEN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114497233 11449723 1 Seizure
114497233 11449723 2 Product used for unknown indication
114497233 11449723 3 Product used for unknown indication
114497233 11449723 4 Product used for unknown indication
114497233 11449723 5 Product used for unknown indication
114497233 11449723 6 Product used for unknown indication
114497233 11449723 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
114497233 11449723 HO
114497233 11449723 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114497233 11449723 Encephalitis
114497233 11449723 Multiple sclerosis relapse
114497233 11449723 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
114497233 11449723 1 201411 0
114497233 11449723 2 201411 201502 0