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
100904068 10090406 8 F 201309 20160926 20140421 20160929 EXP US-PFIZER INC-2014109517 PFIZER 47.00 YR F Y 0.00000 20160929 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
100904068 10090406 1 PS LYRICA PREGABALIN 1 Oral 100 MG, UNK 21446 100 MG CAPSULE, HARD
100904068 10090406 2 SS LYRICA PREGABALIN 1 Oral 100 MG, 2X/DAY N17614 21446 100 MG CAPSULE, HARD BID
100904068 10090406 3 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100904068 10090406 1 Fibromyalgia
100904068 10090406 2 Spinal cord disorder

Outcome of event

Event ID CASEID OUTC COD
100904068 10090406 HO
100904068 10090406 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100904068 10090406 Anal incontinence
100904068 10090406 Clavicle fracture
100904068 10090406 Depression
100904068 10090406 Pain
100904068 10090406 Road traffic accident
100904068 10090406 Suicidal ideation
100904068 10090406 Urinary incontinence

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
100904068 10090406 2 2010 0