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
126903351 12690335 1 I 20160822 20160826 20160826 EXP TR-PFIZER INC-2016399292 PFIZER 21.00 YR M Y 61.00000 KG 20160826 CN TR TR

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
126903351 12690335 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, 2X/DAY Y 20699 75 MG PROLONGED-RELEASE CAPSULE BID
126903351 12690335 2 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 37.5 MG, UNK Y 20699 37.5 MG PROLONGED-RELEASE CAPSULE
126903351 12690335 3 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Y 20699 PROLONGED-RELEASE CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126903351 12690335 1 Agitation
126903351 12690335 2 Palpitations
126903351 12690335 3 Discomfort

Outcome of event

Event ID CASEID OUTC COD
126903351 12690335 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126903351 12690335 Blood cholesterol increased
126903351 12690335 Blood triglycerides increased
126903351 12690335 Hypertension
126903351 12690335 Product use issue
126903351 12690335 Pruritus

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

no results found

Therapies reported

no results found