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
125940081 12594008 1 I 20151029 20151029 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2015-013842 UNITED THERAPEUTICS 65.91 YR F Y 64.85000 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
125940081 12594008 1 PS TYVASO TREPROSTINIL 1 Respiratory (inhalation) 18-54 MICROGRAMS, QID U U 2100695 22387 INHALATION GAS QID
125940081 12594008 2 SS TYVASO TREPROSTINIL 1 UNK U U 2100699 22387 INHALATION GAS
125940081 12594008 3 SS TYVASO TREPROSTINIL 1 UNK U U 22387 INHALATION GAS
125940081 12594008 4 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD SBFT 0 10 MG TABLET QD
125940081 12594008 5 SS LETAIRIS AMBRISENTAN 1 Unknown UNK 1500225A 0 TABLET
125940081 12594008 6 C ADCIRCA TADALAFIL 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125940081 12594008 1 Pulmonary arterial hypertension
125940081 12594008 4 Pulmonary arterial hypertension
125940081 12594008 6 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125940081 12594008 Cough
125940081 12594008 Drug dose omission
125940081 12594008 Productive cough
125940081 12594008 Throat irritation

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
125940081 12594008 1 20151027 0
125940081 12594008 2 20151027 0
125940081 12594008 3 20151029 0
125940081 12594008 4 20150107 0