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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127311481 | 12731148 | 1 | I | 20160831 | 20160911 | 20160911 | PER | PHEH2016US022255 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160912 | CN | US | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127311481 | 12731148 | 1 | PS | FOCALIN | DEXMETHYLPHENIDATE HYDROCHLORIDE | 1 | Unknown | 21278 | |||||||||||
127311481 | 12731148 | 2 | SS | ADDERALL | AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE | 1 | Unknown | 0 | |||||||||||
127311481 | 12731148 | 3 | SS | DAYTRANA | METHYLPHENIDATE | 1 | Unknown | 35 MG, UNK | 80430 | 0 | 35 | MG | PATCH |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127311481 | 12731148 | 1 | Attention deficit/hyperactivity disorder |
127311481 | 12731148 | 2 | Attention deficit/hyperactivity disorder |
127311481 | 12731148 | 3 | Attention deficit/hyperactivity disorder |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127311481 | 12731148 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |