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
122547635 12254763 5 F 2016 20160720 20160411 20160727 EXP US-UNITED THERAPEUTICS-UNT-2016-005527 UNITED THERAPEUTICS 39.45 YR F Y 106.58000 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
122547635 12254763 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.039 ?G/KG, CONTINUING 2100666 21272 .039 UG/KG INJECTION
122547635 12254763 2 SS REMODULIN TREPROSTINIL 1 UNK 2100701 21272 INJECTION
122547635 12254763 3 C ADCIRCA TADALAFIL 1 0
122547635 12254763 4 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122547635 12254763 1 Pulmonary arterial hypertension
122547635 12254763 3 Product used for unknown indication
122547635 12254763 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122547635 12254763 OT
122547635 12254763 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122547635 12254763 Cardiac failure congestive
122547635 12254763 Diarrhoea
122547635 12254763 Dyspnoea
122547635 12254763 Fluid overload
122547635 12254763 Influenza
122547635 12254763 Influenza like illness
122547635 12254763 Infusion site haemorrhage
122547635 12254763 Pneumonia
122547635 12254763 Pruritus
122547635 12254763 Right ventricular failure
122547635 12254763 Somnolence
122547635 12254763 Spinal fracture

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
122547635 12254763 1 20121228 0