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
76399212 7639921 2 F 20160922 20101026 20160928 PER US-PFIZER INC-2010131885 PFIZER 61.00 YR F Y 54.42000 KG 20160928 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
76399212 7639921 1 PS LYRICA PREGABALIN 1 UNK V100914 21446 CAPSULE, HARD
76399212 7639921 2 SS LYRICA PREGABALIN 1 300 MG, 2X/DAY 21446 300 MG CAPSULE, HARD BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
76399212 7639921 1 Neuralgia
76399212 7639921 2 Fibromyalgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
76399212 7639921 Condition aggravated
76399212 7639921 Gastrooesophageal reflux disease
76399212 7639921 Malaise

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

no results found

Therapies reported

no results found