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
126663081 12666308 1 I 2012 20151217 20160818 20160818 PER US-FRI-1000075269 FOREST 0.00 F Y 0.00000 20160818 CN US 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
126663081 12666308 1 PS CELEXA CITALOPRAM HYDROBROMIDE 1 Oral 40 MG 20822 40 MG TABLET QD
126663081 12666308 2 SS CELEXA CITALOPRAM HYDROBROMIDE 1 Oral 20 MG 20822 20 MG TABLET QD
126663081 12666308 3 SS CELEXA CITALOPRAM HYDROBROMIDE 1 Oral 40 MG 0 40 MG TABLET QD
126663081 12666308 4 SS TAGAMET CIMETIDINE 1 Y 0
126663081 12666308 5 C HIZENTRA HUMAN IMMUNOGLOBULIN G 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126663081 12666308 1 Mental disorder
126663081 12666308 4 Ill-defined disorder
126663081 12666308 5 Immune system disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126663081 12666308 Anxiety
126663081 12666308 Drug interaction
126663081 12666308 Feeding disorder
126663081 12666308 Gastritis
126663081 12666308 Hypersensitivity
126663081 12666308 Off label use
126663081 12666308 Weight decreased

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
126663081 12666308 1 1998 2005 0
126663081 12666308 2 2005 2015 0
126663081 12666308 3 201510 0
126663081 12666308 4 2012 201510 0
126663081 12666308 5 2012 0