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
126589181 12658918 1 I 20160803 20160817 20160817 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-122119 RANBAXY 7.00 YR M Y 0.00000 20160817 OT GB GB

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
126589181 12658918 1 PS RISPERIDONE. RISPERIDONE 1 Unknown 0.5 MG, DAILY 77542 .5 MG
126589181 12658918 2 I RISPERIDONE. RISPERIDONE 1 Unknown 1.5 MG, DAILY (OVER 8 WEEKS) Y Y 77542 1.5 MG
126589181 12658918 3 I CONCERTA METHYLPHENIDATE HYDROCHLORIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126589181 12658918 1 Product used for unknown indication
126589181 12658918 2 Product used for unknown indication
126589181 12658918 3 Attention deficit/hyperactivity disorder

Outcome of event

Event ID CASEID OUTC COD
126589181 12658918 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126589181 12658918 Drug interaction
126589181 12658918 Drug withdrawal syndrome
126589181 12658918 Dyskinesia Dyskinesia

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
126589181 12658918 1 200510 0