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
127443191 12744319 1 I 20160907 20160914 20160914 EXP US-ASTRAZENECA-2016SE95955 ASTRAZENECA 0.00 M Y 0.00000 20160915 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
127443191 12744319 1 PS SEROQUEL QUETIAPINE FUMARATE 1 Oral EVERY MORNING U U 20639 FILM-COATED TABLET
127443191 12744319 2 SS ABILIFY ARIPIPRAZOLE 1 Oral U 0
127443191 12744319 3 SS DEPAKOTE DIVALPROEX SODIUM 1 Oral 100.0MG UNKNOWN U 0 100 MG
127443191 12744319 4 C LACTULOSE. LACTULOSE 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127443191 12744319 1 Bipolar disorder

Outcome of event

Event ID CASEID OUTC COD
127443191 12744319 OT
127443191 12744319 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127443191 12744319 Attention deficit/hyperactivity disorder
127443191 12744319 Back pain
127443191 12744319 Depression
127443191 12744319 Drug hypersensitivity
127443191 12744319 Gait disturbance
127443191 12744319 Hepatic failure
127443191 12744319 Memory impairment
127443191 12744319 Neck pain
127443191 12744319 Oppositional defiant disorder
127443191 12744319 Spinal pain
127443191 12744319 Tardive dyskinesia
127443191 12744319 Thyroid disorder
127443191 12744319 Vision blurred

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
127443191 12744319 1 2012 0