Paroxetine Hydrochloride Anhydrous label

Paroxetine Hydrochloride Anhydrous

Paroxetine Hydrochloride Anhydrous Recall

Get an alert when a recall is issued.

Side Effects & Adverse Reactions

Warnings

Do not use

If you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

heart disease
high blood pressure
thyroid disease
diabetes
trouble urinating due to an enlarged prostate gland

Stop use and ask a doctor if

■ you get nervous, dizzy, or sleepless

■ symptoms do not improve within 7 days or are accompanied by fever

Legal Issues

There is currently no legal information available for this drug.

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Uses

Uses

Temporarily relieves

■ nasal congestion due to the common cold, hay fever or other upper respiratory allergies

■ sinus congestion and pressure

Promotes nasal and/or sinus drainage

History

There is currently no drug history available for this drug.

Other Information

There are no additional details available for this product.

Navigate to :

Paroxetine Hydrochloride Anhydrous Recall

Side Effects & Adverse Reactions

FDA Safety Alerts

Manufacturer Warnings

FDA Labeling Changes

Other Information

Trending Topics

Paroxetine Hydrochloride Anhydrous Manufacturers

Direct Rx
No Recall
Paroxetine Hydrochloride Anhydrous | Moore Medical Llc
Directions do not use more than directed