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
126257282 12625728 2 F 20160808 20160805 20160816 EXP US-GLAXOSMITHKLINE-US2016113340 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160816 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
126257282 12625728 1 SS Ambrisentan AMBRISENTAN 1 Unknown 5 MG, UNK 0 5 MG TABLET
126257282 12625728 2 PS FLOLAN EPOPROSTENOL SODIUM 1 Unknown UNK U 20444
126257282 12625728 3 SS ADCIRCA TADALAFIL 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126257282 12625728 1 Product used for unknown indication
126257282 12625728 2 Product used for unknown indication
126257282 12625728 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126257282 12625728 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126257282 12625728 Adrenal insufficiency
126257282 12625728 Body temperature fluctuation
126257282 12625728 Haemoptysis
126257282 12625728 Malaise
126257282 12625728 Mood swings
126257282 12625728 Neoplasm malignant
126257282 12625728 Pulmonary haemorrhage
126257282 12625728 Pulse abnormal
126257282 12625728 Renal disorder

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found