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
125486281 12548628 1 I 20160708 20160712 20160712 EXP US-SCIEGEN PHARMACEUTICALS INC-2016SCILIT00297 SCIEGEN 63.00 YR M Y 0.00000 20160712 MD 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
125486281 12548628 1 PS Fluoxetine Capsules, USP FLUOXETINE HYDROCHLORIDE 1 Unknown UNK U 204597 CAPSULE
125486281 12548628 2 SS LORAZEPAM. LORAZEPAM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125486281 12548628 1 Conversion disorder
125486281 12548628 2 Conversion disorder

Outcome of event

Event ID CASEID OUTC COD
125486281 12548628 HO
125486281 12548628 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125486281 12548628 Aphasia
125486281 12548628 Catatonia
125486281 12548628 Clonus
125486281 12548628 Creutzfeldt-Jakob disease
125486281 12548628 Fall
125486281 12548628 Hyperreflexia
125486281 12548628 Mental status changes
125486281 12548628 Metamorphopsia
125486281 12548628 Movement disorder
125486281 12548628 Myoclonus
125486281 12548628 Paranoia
125486281 12548628 Posturing

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found