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
127151381 12715138 1 I 20160419 20160905 20160905 PER US-ASTRAZENECA-2016SE44104 ASTRAZENECA 0.00 F Y 181.40000 KG 20160906 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
127151381 12715138 1 PS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral U 20639 PROLONGED-RELEASE TABLET
127151381 12715138 2 SS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral U 20639 TABLET
127151381 12715138 3 SS SEROQUEL XR QUETIAPINE FUMARATE 1 Oral SEROQUEL U 20639 TABLET
127151381 12715138 4 SS OTHER MEDICATIONS UNSPECIFIED INGREDIENT 1 Unknown 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127151381 12715138 Back disorder
127151381 12715138 Cardiac failure
127151381 12715138 Depression
127151381 12715138 Glucose tolerance impaired
127151381 12715138 Joint injury
127151381 12715138 Lethargy
127151381 12715138 Somnolence
127151381 12715138 Weight decreased
127151381 12715138 Weight increased

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
127151381 12715138 3 2004 0