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
110910907 11091090 7 F 20160620 20150505 20160705 PER US-PFIZER INC-2015144771 PFIZER 45.00 YR F Y 0.00000 20160705 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
110910907 11091090 1 PS LYRICA PREGABALIN 1 50 MG, 2X/DAY J16127 21446 50 MG BID
110910907 11091090 2 SS LYRICA PREGABALIN 1 21446
110910907 11091090 3 SS LYRICA PREGABALIN 1 21446
110910907 11091090 4 C HYDROXYCHLOROQUINE HYDROXYCHLOROQUINE 1 200 MG, 2X/DAY 0 200 MG BID
110910907 11091090 5 C LOSARTAN AND HYDROCHLOROTHIAZIDE HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM 1 UNK 0
110910907 11091090 6 C LEVOTHYROXINE. LEVOTHYROXINE 1 UNK 0
110910907 11091090 7 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 UNK 0
110910907 11091090 8 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 50 PILLS 2X DAILY 0 BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
110910907 11091090 1 Pain
110910907 11091090 2 Systemic lupus erythematosus
110910907 11091090 3 Fibromyalgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
110910907 11091090 Gait disturbance
110910907 11091090 Malaise
110910907 11091090 Myalgia

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
110910907 11091090 1 20150211 0
110910907 11091090 4 2011 0
110910907 11091090 5 2012 0
110910907 11091090 6 2012 0
110910907 11091090 7 2012 0
110910907 11091090 8 20150211 0