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
126448131 12644813 1 I 2015 20160808 20160811 20160811 PER US-PFIZER INC-2016379894 PFIZER 62.00 YR F Y 81.65000 KG 20160811 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
126448131 12644813 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 35 MG, 3X/DAY U 20699 35 MG PROLONGED-RELEASE CAPSULE TID
126448131 12644813 2 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 150 MG, 1X/DAY IN THE MORNING U 20699 150 MG PROLONGED-RELEASE CAPSULE QD
126448131 12644813 3 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 35 MG 2 CAPSULES ONCE U 20699 70 MG PROLONGED-RELEASE CAPSULE
126448131 12644813 4 C MONTELUKAST MONTELUKAST SODIUM 1 Oral 10 MG, 1X/DAY IN THE EVENING 0 10 MG QD
126448131 12644813 5 C EXEMESTANE. EXEMESTANE 1 Oral 25 MG, 1X/DAY IN THE MORNING 0 25 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126448131 12644813 1 Depression
126448131 12644813 4 Asthma
126448131 12644813 5 Hormone therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126448131 12644813 Balance disorder
126448131 12644813 Dizziness
126448131 12644813 Nausea
126448131 12644813 Peripheral coldness
126448131 12644813 Poor quality sleep
126448131 12644813 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
126448131 12644813 1 2015 201512 0
126448131 12644813 2 2015 20160722 0
126448131 12644813 3 20160801 0
126448131 12644813 5 201405 0