The Safety Rates Drug Report

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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
125952471 12595247 1 I 201512 20151223 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-016376 UNITED THERAPEUTICS 55.80 YR F Y 116.55000 KG 20160726 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
125952471 12595247 1 PS ORENITRAM TREPROSTINIL 1 Oral 0.125 MG, TID U U 2100369 203496 .125 MG TABLET TID
125952471 12595247 2 SS ORENITRAM TREPROSTINIL 1 Oral 0.625 MG, TID U U 2100369 203496 .625 MG TABLET TID
125952471 12595247 3 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100684 203496 TABLET
125952471 12595247 4 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100398 203496 TABLET
125952471 12595247 5 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100397 203496 TABLET
125952471 12595247 6 SS ORENITRAM TREPROSTINIL 1 Oral 1.375 MG, TID U U 2100684 203496 1.375 MG TABLET TID
125952471 12595247 7 SS ORENITRAM TREPROSTINIL 1 Oral 1.875 MG, TID U U 2100397 203496 1.875 MG TABLET TID
125952471 12595247 8 SS ORENITRAM TREPROSTINIL 1 Oral UNK U U 2100477 203496 TABLET
125952471 12595247 9 SS ORENITRAM TREPROSTINIL 1 Oral 0.025 UNK, UNK U U 203496 TABLET
125952471 12595247 10 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD 0 10 MG TABLET QD
125952471 12595247 11 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD 1500225A 0 10 MG TABLET QD
125952471 12595247 12 SS LETAIRIS AMBRISENTAN 1 Oral 10 MG, QD 1500225A 0 10 MG TABLET QD
125952471 12595247 13 SS REVATIO SILDENAFIL CITRATE 1 U U 0
125952471 12595247 14 SS FLOLAN EPOPROSTENOL SODIUM 1 U U 0
125952471 12595247 15 C WARFARIN WARFARIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125952471 12595247 1 Pulmonary arterial hypertension
125952471 12595247 10 Product used for unknown indication
125952471 12595247 13 Product used for unknown indication
125952471 12595247 14 Product used for unknown indication
125952471 12595247 15 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125952471 12595247 Back pain
125952471 12595247 Chronic sinusitis
125952471 12595247 Constipation
125952471 12595247 Feeling abnormal
125952471 12595247 Headache
125952471 12595247 Limb discomfort
125952471 12595247 Nasal congestion
125952471 12595247 Nasal discomfort
125952471 12595247 Nausea
125952471 12595247 Oropharyngeal pain
125952471 12595247 Pain in extremity
125952471 12595247 Pain in jaw
125952471 12595247 Palpitations
125952471 12595247 Restless legs syndrome
125952471 12595247 Sinus congestion

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
125952471 12595247 1 20151209 0
125952471 12595247 10 20071128 0
125952471 12595247 11 20160120 0
125952471 12595247 12 20071107 0