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
100737914 10073791 4 F 20121124 20160803 20140411 20160812 EXP JP-GILEAD-2014-0098949 GILEAD 66.00 YR E F Y 47.00000 KG 20160812 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
100737914 10073791 1 PS AMBRISENTAN AMBRISENTAN 1 Oral 5 MG, QD 32 MG 22081 5 MG TABLET QD
100737914 10073791 2 SS AMBRISENTAN AMBRISENTAN 1 Oral 7.5 MG, QD 32 MG 22081 7.5 MG TABLET QD
100737914 10073791 3 SS AMBRISENTAN AMBRISENTAN 1 Oral 5 MG, QD 32 MG 22081 5 MG TABLET QD
100737914 10073791 4 SS AMBRISENTAN AMBRISENTAN 1 Oral 2.5 MG, QD 32 MG 22081 2.5 MG TABLET QD
100737914 10073791 5 SS REVATIO SILDENAFIL CITRATE 1 Oral UNK 0 TABLET
100737914 10073791 6 SS REVATIO SILDENAFIL CITRATE 1 0 TABLET
100737914 10073791 7 SS FUROSEMIDE. FUROSEMIDE 1 Intravenous (not otherwise specified) UNK Y 0
100737914 10073791 8 SS FUROSEMIDE. FUROSEMIDE 1 Oral UNK Y 0
100737914 10073791 9 C BERASUS BERAPROST SODIUM 1 Oral U 0
100737914 10073791 10 C URSO URSODIOL 1 Oral U 0
100737914 10073791 11 C JUVELA N TOCOPHERYL NICOTINATE, D-.ALPHA. 1 Oral U 0 CAPSULE
100737914 10073791 12 C JUVELA N TOCOPHERYL NICOTINATE, D-.ALPHA. 1 Oral UNK U 0 CAPSULE
100737914 10073791 13 C JUVELA N TOCOPHERYL NICOTINATE, D-.ALPHA. 1 Oral UNK U 0 CAPSULE
100737914 10073791 14 C JUVELA N TOCOPHERYL NICOTINATE, D-.ALPHA. 1 Oral UNK U 0 CAPSULE
100737914 10073791 15 C LIPOVAS /00499301/ FENOFIBRATE 1 Oral U 0
100737914 10073791 16 C Berasus LA 2 Oral 0 TABLET
100737914 10073791 17 C URSO URSODIOL 1 Oral UNK 0 ORAL DRUG UNSPECIFIED FORM
100737914 10073791 18 C LIPOVAS (JAPAN) 2 Oral UNK 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100737914 10073791 1 Pulmonary arterial hypertension
100737914 10073791 2 Pulmonary arterial hypertension
100737914 10073791 5 Pulmonary arterial hypertension
100737914 10073791 6 Pulmonary arterial hypertension
100737914 10073791 7 Product used for unknown indication
100737914 10073791 9 Pulmonary arterial hypertension
100737914 10073791 16 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
100737914 10073791 HO
100737914 10073791 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
100737914 10073791 Breast cancer
100737914 10073791 Hypokalaemia
100737914 10073791 Off label use
100737914 10073791 Pleural effusion
100737914 10073791 Pneumonia
100737914 10073791 Pulmonary oedema

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
100737914 10073791 1 20121114 0
100737914 10073791 2 20120919 20121113 0
100737914 10073791 3 20120822 20120918 0
100737914 10073791 4 20120808 20120821 0
100737914 10073791 7 20121124 20121205 0
100737914 10073791 8 20121206 0