Trelegy and LUNG NEOPLASM MALIGNANT

1 reports of this reaction

4.2% of all Trelegy reports

#16 most reported adverse reaction

Overview

LUNG NEOPLASM MALIGNANT is the #16 most commonly reported adverse reaction for Trelegy, manufactured by Aurobindo Pharma Limited. There are 1 FDA adverse event reports linking Trelegy to LUNG NEOPLASM MALIGNANT. This represents approximately 4.2% of all 24 adverse event reports for this drug.

Patients taking Trelegy who experience lung neoplasm malignant should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

LUNG NEOPLASM MALIGNANT1 of 24 reports

LUNG NEOPLASM MALIGNANT is moderately reported among Trelegy users, representing a notable but not dominant share of adverse events.

Other Side Effects of Trelegy

In addition to lung neoplasm malignant, the following adverse reactions have been reported for Trelegy:

Other Drugs Associated with LUNG NEOPLASM MALIGNANT

The following drugs have also been linked to lung neoplasm malignant in FDA adverse event reports:

CHLOROXYLENOLCRIZOTINIBRANITIDINERANITIDINE HYDROCHLORIDE

Frequently Asked Questions

Does Trelegy cause LUNG NEOPLASM MALIGNANT?

LUNG NEOPLASM MALIGNANT has been reported as an adverse event in 1 FDA reports for Trelegy. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is LUNG NEOPLASM MALIGNANT with Trelegy?

LUNG NEOPLASM MALIGNANT accounts for approximately 4.2% of all adverse event reports for Trelegy, making it a notable side effect.

What should I do if I experience LUNG NEOPLASM MALIGNANT while taking Trelegy?

If you experience lung neoplasm malignant while taking Trelegy, 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.

Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.