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
125982221 12598222 1 I 20150227 20160118 20160727 20160727 PER US-MYLANLABS-2016M1003816 MYLAN 50.11 YR M Y 99.77000 KG 20160727 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
125982221 12598222 1 PS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral 500 MG, QD Y 76276 500 MG QD
125982221 12598222 2 C FLOLAN EPOPROSTENOL SODIUM 1 Unknown UNK U 0
125982221 12598222 3 C FELODIPINE. FELODIPINE 1 Unknown UNK U 0
125982221 12598222 4 C SILDENAFIL. SILDENAFIL 1 Unknown UNK U 0
125982221 12598222 5 C spirolactone SPIRONOLACTONE 1 Unknown UNK U 0
125982221 12598222 6 C BENZONATATE. BENZONATATE 1 Unknown UNK U 0
125982221 12598222 7 C FUROSEMIDE. FUROSEMIDE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125982221 12598222 1 Device related infection
125982221 12598222 2 Pulmonary arterial hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125982221 12598222 Dizziness
125982221 12598222 Drug hypersensitivity
125982221 12598222 Headache
125982221 12598222 Nausea

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
125982221 12598222 1 20150226 20150227 0