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
125209581 12520958 1 I 20120717 20131118 20160701 20160701 EXP JP-GLAXOSMITHKLINE-B0947307A GLAXOSMITHKLINE 18.21 YR M Y 40.00000 KG 20160701 CN JP JP

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
125209581 12520958 1 SS Ambrisentan AMBRISENTAN 1 Oral 65 MG 0 2.5 MG TABLET QD
125209581 12520958 2 SS Ambrisentan AMBRISENTAN 1 Oral 2.5 MG, BID 65 MG 0 2.5 MG TABLET BID
125209581 12520958 3 SS Ambrisentan AMBRISENTAN 1 Oral 5 MG, QD 65 MG 0 5 MG TABLET QD
125209581 12520958 4 PS EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) UNK 20444 SOLUTION FOR INJECTION
125209581 12520958 5 SS EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) UNK 20444 SOLUTION FOR INJECTION
125209581 12520958 6 SS EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) UNK 20444 SOLUTION FOR INJECTION
125209581 12520958 7 SS EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) UNK 20444 SOLUTION FOR INJECTION
125209581 12520958 8 SS EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) UNK 20444 SOLUTION FOR INJECTION
125209581 12520958 9 SS EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) UNK 20444 SOLUTION FOR INJECTION
125209581 12520958 10 SS EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) UNK 20444 SOLUTION FOR INJECTION
125209581 12520958 11 SS EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) UNK 20444 SOLUTION FOR INJECTION
125209581 12520958 12 SS EPOPROSTENOL SODIUM. EPOPROSTENOL SODIUM 1 Intravenous (not otherwise specified) UNK 20444 SOLUTION FOR INJECTION
125209581 12520958 13 SS REVATIO SILDENAFIL CITRATE 1 Oral UNK 0
125209581 12520958 14 SS VANCOMYCIN VANCOMYCIN 1 UNK Y 0
125209581 12520958 15 SS VANCOMYCIN VANCOMYCIN 1 Intravenous (not otherwise specified) UNK Y 0
125209581 12520958 16 C FUROSEMIDE. FUROSEMIDE 1 Oral UNK U 0 ORAL DRUG UNSPECIFIED FORM
125209581 12520958 17 C SPIRONOLACTONE. SPIRONOLACTONE 1 Oral UNK U 0 TABLET
125209581 12520958 18 C Gluconsan K 2 Oral UNK U 0 ORAL DRUG UNSPECIFIED FORM

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125209581 12520958 1 Pulmonary arterial hypertension
125209581 12520958 4 Pulmonary arterial hypertension
125209581 12520958 14 Device related infection
125209581 12520958 16 Pulmonary arterial hypertension
125209581 12520958 17 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
125209581 12520958 HO
125209581 12520958 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125209581 12520958 Device related infection
125209581 12520958 Haemoptysis
125209581 12520958 Red man syndrome

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
125209581 12520958 1 20110526 20120703 0
125209581 12520958 2 20120704 20121128 0
125209581 12520958 3 20121129 0
125209581 12520958 4 20120411 0
125209581 12520958 5 20120411 20120509 0
125209581 12520958 6 20120509 20120606 0
125209581 12520958 7 20120606 20130619 0
125209581 12520958 8 20130619 20130717 0
125209581 12520958 9 20130717 20150220 0
125209581 12520958 10 20150220 20150318 0
125209581 12520958 11 20150318 20150422 0
125209581 12520958 12 20150422 0
125209581 12520958 14 20120719 20120723 0
125209581 12520958 15 20140714 20140714 0