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
125955971 12595597 1 I 201604 20160418 20160726 20160726 PER US-UNITED THERAPEUTICS-UNT-2016-006394 UNITED THERAPEUTICS 71.58 YR F Y 55.78000 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
125955971 12595597 1 PS TYVASO TREPROSTINIL 1 18-54 MICROGRAMS, QID 2100747 22387 INHALATION GAS QID
125955971 12595597 2 SS ADCIRCA TADALAFIL 1 Unknown UNK 0
125955971 12595597 3 SS LETAIRIS AMBRISENTAN 1 Unknown 5 MG, QD SBFS 0 5 MG TABLET QD
125955971 12595597 4 C REVATIO SILDENAFIL CITRATE 1 0
125955971 12595597 5 C DILTIAZEM. DILTIAZEM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125955971 12595597 1 Pulmonary hypertension
125955971 12595597 2 Product used for unknown indication
125955971 12595597 3 Pulmonary hypertension
125955971 12595597 4 Product used for unknown indication
125955971 12595597 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125955971 12595597 Adverse event
125955971 12595597 Cough
125955971 12595597 Dry mouth
125955971 12595597 Eye pain
125955971 12595597 Headache
125955971 12595597 Malaise
125955971 12595597 Palpitations
125955971 12595597 Seasonal allergy
125955971 12595597 Stomatitis

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
125955971 12595597 1 20121127 0
125955971 12595597 3 20160201 0