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Head-to-head · FAERS comparison

Rituximab vs Ocrelizumab: side effects in FDA adverse event reports

How to read this page. FAERS report counts have no denominator; the comparison is of reporting patterns, not of risk. Signals are screened against each FDA label (badges) but not causally assessed. Not medical advice.

At a glance

RituximabOcrelizumab
Drug classCD20-directed Cytolytic AntibodyCD20-directed Cytolytic Antibody
Brand namesRituxanOcrevus
FAERS reports210,13261,582
Serious89%50%
Death outcome37,0691,519
Boxed warningYes FATAL INFUSION-RELATED REACTIONS, SEVERE MUCOCUTANEOUS REACTIONS, HEPATITIS B VIRUS REACTIVATION and PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY WARNING: FATAL INo

Signals both drugs share

No strong shared signal after removing coding and lab terms.

Labeled signals distinctive to Rituximab

Labeled signals distinctive to Ocrelizumab

Common questions

Which has more reported side effects, Rituximab or Ocrelizumab?

Rituximab has 210,132 FAERS reports and Ocrelizumab 61,582. More reports does not mean more dangerous: volume follows how widely and how long a drug has been used, prescription vs over-the-counter status, and publicity. The seriousness share (89% vs 50%) is a better like-for-like signal of the kind of problems reported.

Which side effects do Rituximab and Ocrelizumab share?

They share no strong flagged signal after artifacts and lab terms are removed.

Is Rituximab or Ocrelizumab safer?

FAERS cannot answer that: it has no denominator and no comparator. Use this page to see which risks are already on each label and which signals are unlabeled, then check the prescribing information and your clinician for your situation.

Sources: openFDA FAERS pair statistics (OpenPV build 2026-09-14), FDA labels via openFDA, openFDA count queries for seriousness and deaths. Pair chosen because it is a commonly searched comparison. Generated 2026-10-08.