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Head-to-head · FAERS comparison

Ranitidine vs Loratadine: 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

RanitidineLoratadine
Drug class––
Brand names––
FAERS reports197,701106,935
Serious93%47%
Death outcome15,5204,661
Boxed warningNoNo

Signals both drugs share

ReactionRanitidineLoratadineLabel screen (A / B)
Chronic kidney disease-mineral and bone disorder149 · PRR 16.980 · PRR 15.7Not in label — unassessed / No label text to screen

Labeled signals distinctive to Ranitidine

  • None stood out among the strongest labeled signals.

Labeled signals distinctive to Loratadine

  • None stood out among the strongest labeled signals.

Common questions

Which has more reported side effects, Ranitidine or Loratadine?

Ranitidine has 197,701 FAERS reports and Loratadine 106,935. 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 (93% vs 47%) is a better like-for-like signal of the kind of problems reported.

Which side effects do Ranitidine and Loratadine share?

Both drugs carry disproportionality signals for chronic kidney disease-mineral and bone disorder. Shared signals often reflect a shared drug class or the condition both are used for.

Is Ranitidine or Loratadine 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.