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
126276481 12627648 1 I 2009 20160801 20160805 20160805 EXP GB-ASTRAZENECA-2016SE82869 ASTRAZENECA 51.00 YR F Y 0.00000 20160806 OT GB GB

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
126276481 12627648 1 PS QUETIAPINE. QUETIAPINE 1 Oral N 20639 TABLET
126276481 12627648 2 SS QUETIAPINE. QUETIAPINE 1 Oral N 20639 400 MG TABLET BID
126276481 12627648 3 SS FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 Unknown 100.0MG UNKNOWN N U 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126276481 12627648 3 Anxiety

Outcome of event

Event ID CASEID OUTC COD
126276481 12627648 DE
126276481 12627648 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126276481 12627648 Agitation
126276481 12627648 Asthma
126276481 12627648 Death
126276481 12627648 Drug withdrawal syndrome
126276481 12627648 Interstitial lung disease
126276481 12627648 Overdose
126276481 12627648 Pneumonia
126276481 12627648 Tremor

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
126276481 12627648 3 2008 0