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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

PEGCETACOPLAN for Paroxysmal nocturnal haemoglobinuria: Side Effects & Safety Data

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There are 559 adverse event reports in the FDA FAERS database where PEGCETACOPLAN was used for Paroxysmal nocturnal haemoglobinuria.

Most Reported Side Effects for PEGCETACOPLAN

Side Effect Reports % Deaths Hosp.
Fatigue 135 9.9% 1 44
Visual impairment 125 9.1% 0 4
Haemoglobin decreased 106 7.7% 1 51
Haemolysis 100 7.3% 1 57
Off label use 97 7.1% 9 35
Vitreous floaters 78 5.7% 0 4
Breakthrough haemolysis 67 4.9% 1 18
Headache 66 4.8% 2 25
Product dose omission issue 59 4.3% 2 26
Uveitis 59 4.3% 0 0
Covid-19 56 4.1% 1 21
Vitritis 55 4.0% 0 5
Choroidal neovascularisation 52 3.8% 1 2
Eye inflammation 52 3.8% 0 2
Drug ineffective 49 3.6% 8 15

Other Indications for PEGCETACOPLAN

Product used for unknown indication (352) Dry age-related macular degeneration (326) C3 glomerulopathy (27) Age-related macular degeneration (23) Macular degeneration (13) Neovascular age-related macular degeneration (13)

Other Drugs Used for Paroxysmal nocturnal haemoglobinuria

ECULIZUMAB (12,054) RAVULIZUMAB-CWVZ (2,175) SOLIRIS (1,478) IPTACOPAN (291) DANICOPAN (89) CYCLOSPORINE (50) RAVULIZUMAB (50) CROVALIMAB-AKKZ (36) PREDNISOLONE (17) PREDNISONE (8)

Related Pages

PEGCETACOPLAN Full Profile All Paroxysmal nocturnal haemoglobinuria Drugs PEGCETACOPLAN Demographics PEGCETACOPLAN Timeline