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
127026581 12702658 1 I 20160821 20160825 20160831 20160831 EXP US-SHIRE-US201611290 SHIRE 16.42 YR F Y 0.00000 20160831 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
127026581 12702658 1 PS VYVANSE LISDEXAMFETAMINE DIMESYLATE 1 Oral 50 MG, 1X/DAY:QD (IN A.M.) 21977 50 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127026581 12702658 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127026581 12702658 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127026581 12702658 Abdominal pain upper
127026581 12702658 Anxiety
127026581 12702658 Crying
127026581 12702658 Drug dose omission
127026581 12702658 Headache
127026581 12702658 Malaise
127026581 12702658 Nasal congestion
127026581 12702658 Nausea
127026581 12702658 Nervousness
127026581 12702658 Oropharyngeal pain
127026581 12702658 Pain
127026581 12702658 Poor quality sleep
127026581 12702658 Withdrawal syndrome

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

no results found

Therapies reported

no results found