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
126791192 12679119 2 F 2009 20160809 20160824 20160824 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2015RR-104532 RANBAXY 51.00 YR F Y 0.00000 20160824 MD 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
126791192 12679119 1 PS FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 Unknown 100.0 MG UNKNOWN U 76990 100 MG
126791192 12679119 2 SS QUETIAPINE. QUETIAPINE 1 Oral 400 MG, BID U 0 400 MG Q12H
126791192 12679119 3 SS QUETIAPINE. QUETIAPINE 1 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126791192 12679119 1 Anxiety
126791192 12679119 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126791192 12679119 HO
126791192 12679119 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126791192 12679119 Agitation
126791192 12679119 Asthma
126791192 12679119 Death
126791192 12679119 Drug withdrawal syndrome
126791192 12679119 Interstitial lung disease
126791192 12679119 Overdose
126791192 12679119 Pneumonia
126791192 12679119 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
126791192 12679119 1 2008 0