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
123969672 12396967 2 F 20160429 20160628 20160524 20160705 EXP US-UNITED THERAPEUTICS-UNT-2016-007239 UNITED THERAPEUTICS 57.29 YR F Y 55.78000 KG 20160705 OT 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
123969672 12396967 1 PS REMODULIN TREPROSTINIL 1 Intravenous drip 0.075 ?G/KG, CONTINUING 2100701 21272 .075 UG/KG INJECTION
123969672 12396967 2 SS REMODULIN TREPROSTINIL 1 UNK 31320112B 21272 INJECTION
123969672 12396967 3 C REVATIO SILDENAFIL CITRATE 1 0
123969672 12396967 4 C TORSEMIDE. TORSEMIDE 1 0
123969672 12396967 5 C SPIRONOLACTONE. SPIRONOLACTONE 1 0
123969672 12396967 6 C METOLAZONE. METOLAZONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123969672 12396967 1 Pulmonary arterial hypertension
123969672 12396967 3 Product used for unknown indication
123969672 12396967 4 Product used for unknown indication
123969672 12396967 5 Product used for unknown indication
123969672 12396967 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123969672 12396967 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123969672 12396967 Chest pain
123969672 12396967 Device dislocation
123969672 12396967 Drug dose omission

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
123969672 12396967 1 20140221 0