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
123409533 12340953 3 F 20160711 20160506 20160715 EXP US-PFIZER INC-2016247262 PFIZER 26.00 YR F Y 104.00000 KG 20160715 OT 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
123409533 12340953 1 PS VENLAFAXINE HCL VENLAFAXINE HYDROCHLORIDE 1 Oral 150 MG, DAILY Y 20699 150 MG PROLONGED-RELEASE CAPSULE
123409533 12340953 2 C ADDERALL AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE 1 25 MG, 1X/DAY 0 25 MG QD
123409533 12340953 3 C SINGULAIR MONTELUKAST SODIUM 1 10 MG, 1X/DAY 0 10 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123409533 12340953 1 Depression
123409533 12340953 2 Attention deficit/hyperactivity disorder
123409533 12340953 3 Hypersensitivity

Outcome of event

Event ID CASEID OUTC COD
123409533 12340953 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123409533 12340953 Abdominal discomfort
123409533 12340953 Condition aggravated
123409533 12340953 Depression
123409533 12340953 Drug ineffective
123409533 12340953 Headache
123409533 12340953 Hyperhidrosis
123409533 12340953 Mood altered
123409533 12340953 Pyrexia
123409533 12340953 Sleep disorder
123409533 12340953 Suicidal ideation
123409533 12340953 Vomiting
123409533 12340953 Withdrawal syndrome

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
123409533 12340953 2 2008 0
123409533 12340953 3 2006 0