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
125831981 12583198 1 I 2015 20160719 20160722 20160722 EXP US-GLAXOSMITHKLINE-US2016GSK104132 GLAXOSMITHKLINE 39.39 YR F Y 0.00000 20160722 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
125831981 12583198 1 PS LAMICTAL LAMOTRIGINE 1 UNK, U Y 20241
125831981 12583198 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous 40 MG, EVERY 2 WEEKS Y 0 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
125831981 12583198 3 SS RITALIN METHYLPHENIDATE HYDROCHLORIDE 1 Subcutaneous UNK, U Y 0
125831981 12583198 4 SS KLONOPIN CLONAZEPAM 1 UNK,U Y 0
125831981 12583198 5 C ATIVAN LORAZEPAM 1 0
125831981 12583198 6 C LATUDA LURASIDONE HYDROCHLORIDE 1 0
125831981 12583198 7 C PRAZOSIN PRAZOSIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125831981 12583198 1 Bipolar disorder
125831981 12583198 2 Psoriatic arthropathy
125831981 12583198 3 Product used for unknown indication
125831981 12583198 4 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125831981 12583198 OT
125831981 12583198 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125831981 12583198 Confusional state
125831981 12583198 Injection site bruising
125831981 12583198 Loss of consciousness
125831981 12583198 Therapy change

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
125831981 12583198 2 2015 0
125831981 12583198 3 2001 0
125831981 12583198 4 2001 0