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
126054621 12605462 1 I 201601 20160122 20160729 20160729 PER US-UNITED THERAPEUTICS-UNT-2016-001185 UNITED THERAPEUTICS 66.37 YR M Y 88.44000 KG 20160729 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
126054621 12605462 1 PS TYVASO TREPROSTINIL 1 18-54 MICROGRAMS, QID U U 2100711 22387 INHALATION GAS
126054621 12605462 2 SS TYVASO TREPROSTINIL 1 UNK U U 2100747 22387 INHALATION GAS
126054621 12605462 3 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD 1500225A 0 10 MG TABLET QD
126054621 12605462 4 SS ADCIRCA TADALAFIL 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126054621 12605462 1 Pulmonary arterial hypertension
126054621 12605462 3 Product used for unknown indication
126054621 12605462 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126054621 12605462 Gout
126054621 12605462 Oedema peripheral
126054621 12605462 Pain in extremity

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
126054621 12605462 1 20121018 0
126054621 12605462 3 20071023 0