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
126464651 12646465 1 I 20160802 20160812 20160812 PER US-ASTRAZENECA-2016SE84890 ASTRAZENECA 0.00 M Y 0.00000 20160812 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
126464651 12646465 1 PS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral 22047 400 MG PROLONGED-RELEASE TABLET QD
126464651 12646465 2 SS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral 22047 400 MG PROLONGED-RELEASE TABLET QD
126464651 12646465 3 SS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral 22047 200 MG PROLONGED-RELEASE TABLET QD
126464651 12646465 4 SS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral 22047 200 MG PROLONGED-RELEASE TABLET QD
126464651 12646465 5 C LAMICTAL LAMOTRIGINE 1 200 MG 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126464651 12646465 1 Mental disorder
126464651 12646465 2 Affective disorder
126464651 12646465 3 Mental disorder
126464651 12646465 4 Affective disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126464651 12646465 Dysphagia
126464651 12646465 Off label use
126464651 12646465 Product use issue

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
126464651 12646465 1 20160526 0
126464651 12646465 2 20160526 0
126464651 12646465 3 20160526 0
126464651 12646465 4 20160526 0