NORETHINDRONE and PELVIC PAIN

181 reports of this reaction

1.6% of all NORETHINDRONE reports

#17 most reported adverse reaction

Overview

PELVIC PAIN is the #17 most commonly reported adverse reaction for NORETHINDRONE, manufactured by Amneal Pharmaceuticals LLC. There are 181 FDA adverse event reports linking NORETHINDRONE to PELVIC PAIN. This represents approximately 1.6% of all 11,560 adverse event reports for this drug.

Patients taking NORETHINDRONE who experience pelvic pain 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

PELVIC PAIN181 of 11,560 reports

PELVIC PAIN is a less commonly reported adverse event for NORETHINDRONE, but still significant enough to appear in the safety profile.

Other Side Effects of NORETHINDRONE

In addition to pelvic pain, the following adverse reactions have been reported for NORETHINDRONE:

Other Drugs Associated with PELVIC PAIN

The following drugs have also been linked to pelvic pain in FDA adverse event reports:

COPPERLEVONORGESTRELNORETHINDRONE ACETATE

Frequently Asked Questions

Does NORETHINDRONE cause PELVIC PAIN?

PELVIC PAIN has been reported as an adverse event in 181 FDA reports for NORETHINDRONE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is PELVIC PAIN with NORETHINDRONE?

PELVIC PAIN accounts for approximately 1.6% of all adverse event reports for NORETHINDRONE, making it a notable side effect.

What should I do if I experience PELVIC PAIN while taking NORETHINDRONE?

If you experience pelvic pain while taking NORETHINDRONE, 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.

Related Pages

NORETHINDRONE Full ProfileAll Drugs Causing PELVIC PAINAmneal Pharmaceuticals LLC Drugs
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.