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
124199602 12419960 2 F 2016 20160628 20160531 20160712 EXP US-VALIDUS PHARMACEUTICALS LLC-US-2016VAL001619 VALIDUS 0.00 Y 0.00000 20160711 OT 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
124199602 12419960 1 PS LASIX FUROSEMIDE 1 UNK 16273
124199602 12419960 2 SS REMODULIN TREPROSTINIL 1 Intravenous drip 0.040 ?G/KG, CONTINUING 2100579 0 .04 UG/KG INJECTION
124199602 12419960 3 SS REVATIO SILDENAFIL CITRATE 1 2 DF, TID 0 2 DF TABLET
124199602 12419960 4 C COUMADIN WARFARIN SODIUM 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124199602 12419960 1 Product used for unknown indication
124199602 12419960 2 Pulmonary hypertension
124199602 12419960 3 Product used for unknown indication
124199602 12419960 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124199602 12419960 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124199602 12419960 Blood pressure abnormal
124199602 12419960 Fall
124199602 12419960 Sepsis
124199602 12419960 Urinary tract infection

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
124199602 12419960 2 20121010 0