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
126299212 12629921 2 F 20160705 20160804 20160808 20160816 EXP DE-FRI-1000086680 FOREST 42.68 YR F Y 0.00000 20160816 OT DK DE

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
126299212 12629921 1 PS ESCITALOPRAM ESCITALOPRAM OXALATE 1 Oral 10 MG 2488315 21323 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126299212 12629921 1 Post-traumatic stress disorder

Outcome of event

Event ID CASEID OUTC COD
126299212 12629921 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126299212 12629921 Dizziness
126299212 12629921 Dysuria
126299212 12629921 Increased appetite
126299212 12629921 Malaise
126299212 12629921 Micturition disorder
126299212 12629921 Micturition urgency
126299212 12629921 Muscular weakness
126299212 12629921 Nausea
126299212 12629921 Paraesthesia
126299212 12629921 Product use issue
126299212 12629921 Pruritus
126299212 12629921 Sexual dysfunction
126299212 12629921 Somnolence
126299212 12629921 Tremor
126299212 12629921 Urinary retention
126299212 12629921 Urticaria
126299212 12629921 Weight increased

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
126299212 12629921 1 20160705 0