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
103817261 10381726 1 I 2014 20140805 20140813 20140813 EXP US-ASTRAZENECA-2014SE56826 ASTRAZENECA 50.00 YR F Y 117.90000 KG 20140813 N AF 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
103817261 10381726 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 ORAL 160-4.5, UNKNOWN D 21929
103817261 10381726 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 ORAL 80-4.5, UNKNOWN D 21929
103817261 10381726 3 SS SEROQUEL QUETIAPINE FUMARATE 1 ORAL D 0 50 MG TABLET
103817261 10381726 4 SS SEROQUEL QUETIAPINE FUMARATE 1 ORAL D 0 50 MG TABLET
103817261 10381726 5 C LAMICTAL LAMOTRIGINE 1 ORAL D 0 100 MG BID
103817261 10381726 6 C ZANEX 2 ORAL D 0 2 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103817261 10381726 1 Chronic obstructive pulmonary disease
103817261 10381726 2 Chronic obstructive pulmonary disease
103817261 10381726 3 Bipolar disorder
103817261 10381726 4 Sleep disorder
103817261 10381726 5 Bipolar disorder
103817261 10381726 6 Bipolar disorder

Outcome of event

Event ID CASEID OUTC COD
103817261 10381726 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
103817261 10381726 Bipolar disorder
103817261 10381726 Dyspnoea
103817261 10381726 Intentional product misuse

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
103817261 10381726 1 201003 0
103817261 10381726 2 201003 201406 0
103817261 10381726 3 2014 0
103817261 10381726 4 2014 0