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
126484541 12648454 1 I 201604 20160809 20160812 20160812 EXP PHHY2016BR110423 NOVARTIS 0.00 M Y 86.00000 KG 20160812 OT 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
126484541 12648454 1 PS RITALIN LA METHYLPHENIDATE HYDROCHLORIDE 1 Oral 1 DF, QD Y U 21284 1 DF EXTENDED RELEASE CAPSULES QD
126484541 12648454 2 C PANTOPRAZOLE PANTOPRAZOLE SODIUM 1 Oral 1 DF, QD 0 1 DF QD
126484541 12648454 3 C RIVOTRIL CLONAZEPAM 1 Oral 1 DF, QD 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126484541 12648454 1 Psychomotor hyperactivity
126484541 12648454 2 Gastrooesophageal reflux disease
126484541 12648454 3 Anxiety

Outcome of event

Event ID CASEID OUTC COD
126484541 12648454 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126484541 12648454 Anxiety
126484541 12648454 Dizziness
126484541 12648454 Dry mouth
126484541 12648454 Headache

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
126484541 12648454 1 201604 201605 0