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
125480691 12548069 1 I 20160630 20160712 20160712 EXP PHEH2016US016813 NOVARTIS 0.00 M Y 0.00000 20160712 CN COUNTRY NOT SPECIFIED US

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
125480691 12548069 1 PS RITALIN METHYLPHENIDATE HYDROCHLORIDE 1 Unknown UNK 10187
125480691 12548069 2 SS ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 Unknown UNK 0
125480691 12548069 3 C MULTI VIT 2 Unknown U 0
125480691 12548069 4 C VITAMIIN C ASCORBIC ACID 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125480691 12548069 1 Attention deficit/hyperactivity disorder
125480691 12548069 2 Attention deficit/hyperactivity disorder
125480691 12548069 3 Product used for unknown indication
125480691 12548069 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125480691 12548069 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125480691 12548069 Crying
125480691 12548069 Drug administered to patient of inappropriate age
125480691 12548069 Dyspepsia
125480691 12548069 Feeding disorder
125480691 12548069 Insomnia
125480691 12548069 Restlessness
125480691 12548069 Weight decreased

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

no results found

Therapies reported

no results found