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
127151901 12715190 1 I 2010 20160829 20160905 20160905 EXP BR-ROCHE-1822887 ROCHE 0.00 F Y 0.00000 20160906 CN BR BR

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
127151901 12715190 1 PS RIVOTRIL CLONAZEPAM 1 Unknown Y RJ1000 17533 .5 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127151901 12715190 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127151901 12715190 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127151901 12715190 Agitation
127151901 12715190 Blindness
127151901 12715190 Dizziness
127151901 12715190 Drug ineffective
127151901 12715190 Fall
127151901 12715190 Gait disturbance
127151901 12715190 Gingival erythema
127151901 12715190 Gingival pain
127151901 12715190 Glossodynia
127151901 12715190 Muscular weakness
127151901 12715190 Pain in extremity
127151901 12715190 Poor quality sleep
127151901 12715190 Sinusitis
127151901 12715190 Urinary incontinence
127151901 12715190 Vertigo

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
127151901 12715190 1 201608 0