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
96957803 9695780 3 F 20120726 20140617 20131119 20160705 PER JP-FRI-1000051453 FOREST 29.67 YR M Y 80.00000 KG 20160705 OT DK JP

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
96957803 9695780 1 PS LEXAPRO ESCITALOPRAM OXALATE 1 Oral U 21323
96957803 9695780 2 SS LEXAPRO ESCITALOPRAM OXALATE 1 Oral U 21323 150 MG
96957803 9695780 3 C MEILAX ETHYL LOFLAZEPATE 1 Oral 0
96957803 9695780 4 C ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 Oral 60 G 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
96957803 9695780 1 Hyperhidrosis

Outcome of event

Event ID CASEID OUTC COD
96957803 9695780 OT
96957803 9695780 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
96957803 9695780 Depressed level of consciousness
96957803 9695780 Hyperhidrosis
96957803 9695780 Intentional overdose
96957803 9695780 Off label use
96957803 9695780 Pyrexia
96957803 9695780 Rhabdomyolysis
96957803 9695780 Suicide attempt
96957803 9695780 Tachycardia

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
96957803 9695780 1 20120726 0
96957803 9695780 2 20130923 0