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
126504982 12650498 2 F 20160711 20160907 20160815 20160907 EXP FR-ROCHE-1812413 ROCHE 12.00 YR M Y 151.00000 KG 20160908 MD FR FR

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
126504982 12650498 1 PS RIVOTRIL CLONAZEPAM 1 Oral U 17533 2 MG TABLET Q2H
126504982 12650498 2 C RISPERDAL RISPERIDONE 1 0
126504982 12650498 3 C MELATONIN MELATONIN 1 0
126504982 12650498 4 C RITALIN METHYLPHENIDATE HYDROCHLORIDE 1 Unknown 0 10 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126504982 12650498 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126504982 12650498 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126504982 12650498 Ataxia
126504982 12650498 Drug dispensing error
126504982 12650498 Hyperventilation
126504982 12650498 Salivary hypersecretion
126504982 12650498 Somnolence

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
126504982 12650498 1 20160711 20160711 0