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
126906371 12690637 1 I 201608 20160823 20160826 20160826 EXP US-PFIZER INC-2016400497 PFIZER 43.00 YR F Y 104.00000 KG 20160826 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
126906371 12690637 1 PS SKELAXIN METAXALONE 1 Oral 800 MG, 2X/DAY U 113676 13217 800 MG TABLET BID
126906371 12690637 2 SS SKELAXIN METAXALONE 1 U 13217 TABLET
126906371 12690637 3 SS LYRICA PREGABALIN 1 Oral 150 MG, 2X/DAY U N46086 21446 150 MG CAPSULE, HARD BID
126906371 12690637 4 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral 150 MG, 2X/DAY U M27075 20699 150 MG PROLONGED-RELEASE CAPSULE BID
126906371 12690637 5 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 U 20699 PROLONGED-RELEASE CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126906371 12690637 1 Pain
126906371 12690637 2 Hypotonia
126906371 12690637 3 Fibromyalgia
126906371 12690637 4 Depression
126906371 12690637 5 Anxiety

Outcome of event

Event ID CASEID OUTC COD
126906371 12690637 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126906371 12690637 Cholelithiasis
126906371 12690637 Nausea

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

no results found

Therapies reported

no results found