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
125609062 12560906 2 F 201404 20160707 20160715 20160722 EXP CA-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-120285 RANBAXY 18.00 YR F Y 0.00000 20160722 OT GB CA

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
125609062 12560906 1 PS AMITRIPTYLINE AMITRIPTYLINE 1 Oral 100MG (EACH BOTTLE HELD APPROXIMATELY 60 TABLETS) U 40816 TABLET
125609062 12560906 2 I DESVENLAFAXINE. DESVENLAFAXINE 1 Oral 100MG (EACH BOTTLE HELD APPROXIMATELY 60 TABLETS) U 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125609062 12560906 1 Depression
125609062 12560906 2 Depression

Outcome of event

Event ID CASEID OUTC COD
125609062 12560906 HO
125609062 12560906 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125609062 12560906 Drug interaction
125609062 12560906 Electrocardiogram QRS complex prolonged
125609062 12560906 Electrocardiogram QT prolonged
125609062 12560906 Intentional overdose
125609062 12560906 Suicide attempt
125609062 12560906 Unresponsive to stimuli

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
125609062 12560906 1 201404 0
125609062 12560906 2 201404 0