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
126616391 12661639 1 I 20160709 20160802 20160817 20160817 PER US-ASTRAZENECA-2016SE84457 ASTRAZENECA 0.00 F Y 0.00000 20160817 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
126616391 12661639 1 PS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral U 20639 300 MG PROLONGED-RELEASE TABLET QD
126616391 12661639 2 C LEXAPRO ESCITALOPRAM OXALATE 1 Oral 0 5 MG QD
126616391 12661639 3 C LEXAPRO ESCITALOPRAM OXALATE 1 Oral 0 2.5 MG QD
126616391 12661639 4 C ARMOUR THYROID THYROID, PORCINE 1 Oral 0 60 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126616391 12661639 1 Bipolar disorder
126616391 12661639 2 Depression
126616391 12661639 3 Depression
126616391 12661639 4 Hypothyroidism

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126616391 12661639 Agitation
126616391 12661639 Insomnia
126616391 12661639 Nervousness
126616391 12661639 Therapy cessation
126616391 12661639 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
126616391 12661639 1 20160801 0