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
125948821 12594882 1 I 20160622 20160726 20160726 EXP BR-PFIZER INC-2016315324 PFIZER 0.00 F Y 0.00000 20160726 MD BR BR

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
125948821 12594882 1 PS ZYVOX LINEZOLID 1 Oral 600 MG EVERY 12 HOURS Y 21131 600 MG BID
125948821 12594882 2 C RIVOTRIL CLONAZEPAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125948821 12594882 1 Device related infection
125948821 12594882 2 Sleep disorder

Outcome of event

Event ID CASEID OUTC COD
125948821 12594882 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125948821 12594882 Burn oral cavity
125948821 12594882 Decreased appetite
125948821 12594882 Dehydration
125948821 12594882 Depression
125948821 12594882 Dysphagia
125948821 12594882 Mucosal hyperaemia
125948821 12594882 Nausea
125948821 12594882 Oral pain
125948821 12594882 Pain
125948821 12594882 Somnolence
125948821 12594882 Stomatitis
125948821 12594882 Vision blurred
125948821 12594882 Vomiting
125948821 12594882 Weight decreased

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

no results found

Therapies reported

no results found