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
126339561 12633956 1 I 201607 20160728 20160808 20160808 PER US-PFIZER INC-2016366976 PFIZER 80.00 YR F Y 46.26000 KG 20160808 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
126339561 12633956 1 PS ZYVOX LINEZOLID 1 600MG ONCE DAILY FOR 7 DAYS 21130 600 MG FILM-COATED TABLET
126339561 12633956 2 C LEVODOPA-CARBIDOPA CARBIDOPALEVODOPA 1 Oral [CARBIDOPA 25MG]/[LEVODOPA 100MG]ONE TABLET THREE TIMES DAILY 0 1 DF TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126339561 12633956 1 Urinary tract infection enterococcal
126339561 12633956 2 Parkinson's disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126339561 12633956 Blood pressure increased
126339561 12633956 Confusional state
126339561 12633956 Fatigue
126339561 12633956 Myalgia
126339561 12633956 Off label use

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
126339561 12633956 1 201607 201607 0
126339561 12633956 2 2013 201607 0