The Safety Rates Drug Report

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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
127774821 12777482 1 I 20151002 20160924 20160924 PER US-TEVA-599190USA TEVA 0.00 M Y 0.00000 20160924 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
127774821 12777482 1 PS CLONAZEPAM. CLONAZEPAM 1 1.5 MILLIGRAM DAILY; Y 74569 .5 MG TID
127774821 12777482 2 SS CLONAZEPAM. CLONAZEPAM 1 .5 MILLIGRAM DAILY; Y 74569 .5 MG QD
127774821 12777482 3 SS CLONAZEPAM. CLONAZEPAM 1 Y 74569

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127774821 12777482 1 Panic disorder
127774821 12777482 2 Restless legs syndrome
127774821 12777482 3 Chronic fatigue syndrome

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127774821 12777482 Abdominal discomfort Abdominal discomfort
127774821 12777482 Abdominal distension Abdominal distension
127774821 12777482 Dizziness Dizziness
127774821 12777482 Feeling abnormal Feeling abnormal
127774821 12777482 Nervousness Nervousness
127774821 12777482 Visual impairment Visual impairment

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

no results found

Therapies reported

no results found