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
116778204 11677820 4 F 2009 20160801 20151028 20160815 EXP GB-MHRA-ADR 23161713 GB-WATSON-2015-21240 ACTAVIS 0.00 Y 0.00000 20160815 CN 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
116778204 11677820 1 SS FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 Unknown 100 MG, UNK UNCONFIRMED 0 100 MG UNK
116778204 11677820 2 PS Quetiapine (Unknown) QUETIAPINE 1 Unknown 400 MG, BID UNCONFIRMED 201762 400 MG UNK BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116778204 11677820 1 Anxiety
116778204 11677820 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
116778204 11677820 HO
116778204 11677820 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
116778204 11677820 Agitation
116778204 11677820 Asthma
116778204 11677820 Death
116778204 11677820 Drug withdrawal syndrome
116778204 11677820 Interstitial lung disease
116778204 11677820 Overdose
116778204 11677820 Pneumonia
116778204 11677820 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
116778204 11677820 1 2008 0