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
126819451 12681945 1 I 20160815 20160824 20160824 EXP US-TEVA-686076USA TEVA 53.00 YR F Y 0.00000 20160824 OT 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
126819451 12681945 1 PS ALBUTEROL. ALBUTEROL 1 Unknown U 21457
126819451 12681945 2 SS REXULTI BREXPIPRAZOLE 1 Unknown Y 0 .5 MG
126819451 12681945 3 SS REXULTI BREXPIPRAZOLE 1 Unknown Y 0 1 MG
126819451 12681945 4 C texapra 2 0
126819451 12681945 5 C ATIVAN LORAZEPAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126819451 12681945 2 Major depression

Outcome of event

Event ID CASEID OUTC COD
126819451 12681945 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126819451 12681945 Hallucination
126819451 12681945 Hypersensitivity
126819451 12681945 Nausea
126819451 12681945 Pharyngeal oedema
126819451 12681945 Urticaria
126819451 12681945 Vomiting

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
126819451 12681945 1 2016 20160718 0
126819451 12681945 2 2016 0
126819451 12681945 3 2016 0