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
126491361 12649136 1 I 20160801 20160812 20160812 PER US-TEVA-681957USA TEVA 0.00 M Y 110.32000 KG 20160812 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
126491361 12649136 1 PS NUVIGIL ARMODAFINIL 1 Unknown U UNKNOWN 21875
126491361 12649136 2 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Unknown 0
126491361 12649136 3 C PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126491361 12649136 1 Attention deficit/hyperactivity disorder
126491361 12649136 2 Attention deficit/hyperactivity disorder
126491361 12649136 3 Attention deficit/hyperactivity disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126491361 12649136 Gastrointestinal injury
126491361 12649136 Hiatus hernia
126491361 12649136 Intestinal cyst
126491361 12649136 Off label use

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

no results found

Therapies reported

no results found