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
99139394 9913939 4 F 20160825 20140220 20160829 EXP US-PFIZER INC-2014036140 PFIZER 57.00 YR M Y 0.00000 20160829 MD 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
99139394 9913939 1 PS LYRICA PREGABALIN 1 UNK U 21446 CAPSULE, HARD
99139394 9913939 2 SS LYRICA PREGABALIN 1 Oral 75 MG, 3X/DAY U 21446 75 MG CAPSULE, HARD TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99139394 9913939 1 Diabetic neuropathy

Outcome of event

Event ID CASEID OUTC COD
99139394 9913939 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
99139394 9913939 Abnormal dreams
99139394 9913939 Cold sweat
99139394 9913939 Coronary artery disease
99139394 9913939 Decreased appetite
99139394 9913939 Insomnia
99139394 9913939 Nausea

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
99139394 9913939 1 20140211 0
99139394 9913939 2 20160824 0