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
125911542 12591154 2 F 20160303 20160324 20160726 20160727 PER US-UNITED THERAPEUTICS-UNT-2016-004430 UNITED THERAPEUTICS 60.00 YR F Y 0.00000 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
125911542 12591154 1 PS REMODULIN TREPROSTINIL 1 Subcutaneous 0.016 ?G/KG, CONTINUING 2100580 21272 .016 UG/KG INJECTION
125911542 12591154 2 SS LETAIRIS AMBRISENTAN 1 Unknown 10 MG, QD 1500225A 0 10 MG TABLET QD
125911542 12591154 3 C LASIX FUROSEMIDE 1 0
125911542 12591154 4 C LYRICA PREGABALIN 1 0
125911542 12591154 5 C PLAQUENIL /00072602/ HYDROXYCHLOROQUINE DIPHOSPHATE 1 0
125911542 12591154 6 C ASPIRIN 81 ASPIRIN 1 0
125911542 12591154 7 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
125911542 12591154 8 C PLAVIX CLOPIDOGREL BISULFATE 1 0
125911542 12591154 9 C PANTOPRAZOLE SODIUM. PANTOPRAZOLE SODIUM 1 0
125911542 12591154 10 C PROCARDIA NIFEDIPINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125911542 12591154 1 Pulmonary arterial hypertension
125911542 12591154 2 Pulmonary hypertension
125911542 12591154 3 Product used for unknown indication
125911542 12591154 4 Product used for unknown indication
125911542 12591154 5 Product used for unknown indication
125911542 12591154 6 Product used for unknown indication
125911542 12591154 7 Product used for unknown indication
125911542 12591154 8 Product used for unknown indication
125911542 12591154 9 Product used for unknown indication
125911542 12591154 10 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125911542 12591154 Device dislocation
125911542 12591154 Drug dose omission
125911542 12591154 Infusion site infection

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
125911542 12591154 1 20160105 0
125911542 12591154 2 20141104 0