AIR and SINUS TACHYCARDIA

3 reports of this reaction

3.4% of all AIR reports

#2 most reported adverse reaction

Overview

SINUS TACHYCARDIA is the #2 most commonly reported adverse reaction for AIR, manufactured by Strate Welding Supply Co., Inc.. There are 3 FDA adverse event reports linking AIR to SINUS TACHYCARDIA. This represents approximately 3.4% of all 87 adverse event reports for this drug.

Patients taking AIR who experience sinus tachycardia 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

SINUS TACHYCARDIA3 of 87 reports

SINUS TACHYCARDIA is moderately reported among AIR users, representing a notable but not dominant share of adverse events.

Other Side Effects of AIR

In addition to sinus tachycardia, the following adverse reactions have been reported for AIR:

Other Drugs Associated with SINUS TACHYCARDIA

The following drugs have also been linked to sinus tachycardia in FDA adverse event reports:

HYOSCYAMUS NIGERPOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL

Frequently Asked Questions

Does AIR cause SINUS TACHYCARDIA?

SINUS TACHYCARDIA has been reported as an adverse event in 3 FDA reports for AIR. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is SINUS TACHYCARDIA with AIR?

SINUS TACHYCARDIA accounts for approximately 3.4% of all adverse event reports for AIR, making it one of the most commonly reported side effect.

What should I do if I experience SINUS TACHYCARDIA while taking AIR?

If you experience sinus tachycardia while taking AIR, 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

AIR Full ProfileAll Drugs Causing SINUS TACHYCARDIAStrate Welding Supply Co., Inc. 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.