321 reports of this reaction
1.4% of all PATIROMER reports
#19 most reported adverse reaction
PRODUCT DOSE OMISSION is the #19 most commonly reported adverse reaction for PATIROMER, manufactured by Vifor Pharma, Inc.. There are 321 FDA adverse event reports linking PATIROMER to PRODUCT DOSE OMISSION. This represents approximately 1.4% of all 23,545 adverse event reports for this drug.
Patients taking PATIROMER who experience product dose omission should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRODUCT DOSE OMISSION is a less commonly reported adverse event for PATIROMER, but still significant enough to appear in the safety profile.
In addition to product dose omission, the following adverse reactions have been reported for PATIROMER:
The following drugs have also been linked to product dose omission in FDA adverse event reports:
PRODUCT DOSE OMISSION has been reported as an adverse event in 321 FDA reports for PATIROMER. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT DOSE OMISSION accounts for approximately 1.4% of all adverse event reports for PATIROMER, making it a notable side effect.
If you experience product dose omission while taking PATIROMER, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.