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
126657872 12665787 2 F 20160902 20160818 20160909 EXP PHHY2016BR110118 NOVARTIS 0.00 F Y 0.00000 20160909 MD 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
126657872 12665787 1 PS RITALIN LA METHYLPHENIDATE HYDROCHLORIDE 1 Oral 20 MG, UNK U FA440 21284 20 MG EXTENDED RELEASE CAPSULES
126657872 12665787 2 SS RITALIN LA METHYLPHENIDATE HYDROCHLORIDE 1 Oral 40 MG, UNK U FA442 21284 40 MG EXTENDED RELEASE CAPSULES
126657872 12665787 3 SS RITALIN LA METHYLPHENIDATE HYDROCHLORIDE 1 U 21284 EXTENDED RELEASE CAPSULES

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126657872 12665787 1 Attention deficit/hyperactivity disorder
126657872 12665787 2 Panic disorder
126657872 12665787 3 Anxiety

Outcome of event

Event ID CASEID OUTC COD
126657872 12665787 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126657872 12665787 Drug dependence
126657872 12665787 Panic disorder
126657872 12665787 Product container seal issue
126657872 12665787 Product use issue

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

no results found

Therapies reported

no results found