Tudorza Pressair Inhalation Powder 400Mcg Drug Medication Dosage Information
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TUDORZA PRESSAIR: Inhalation powder (400mcg)

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Tudorza Pressair 400mcg/act In
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Tudorza Pressair 400mcg/act In
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Tudorza Pressair 400mcg/act In

What is this Medicine?

Aclidinium (a kli DIN ee um) is a bronchodilator. It helps open up the airways in your lungs to make it easier to breathe. This medicine is used to treat COPD, including emphysema and chronic bronchitis. Never use this medicine for an acute attack.

CVS Pharmacy Patient Statistics for TUDORZA PRESSAIR: Inhalation powder(400mcg)
Generic vs. Brand Name Usage*
*Brand contains same active ingredient but may not represent FDA-approved generic equivalent
Usage By Strength
In-Depth Information
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Tudorza Pressair 400mcg/actuation Powder for Inhalation

NDC: 003100800
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Emphysema, Chronic Obstructive Pulmonary Disease (COPD)

Storage Information
Store in a dry place
Store at 77 degrees F; excursions permitted to 59-86 degrees F
Tudorza Pressair 400mcg/actuation Powder for Inhalation

Reported Side Effects for Tudorza Pressair 400mcg/actuation Powder for Inhalation

Dry Mouth Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Heart Failure Incidence:
<1.0%*
Severity: SEVERE
Onset: DELAYED
Diabetes Incidence:
<1.0%*
Severity: MODERATE
Onset: DELAYED
Suddenly Stopped Heart Incidence:
<1.0%*
Severity: SEVERE
Onset: EARLY
Heart Block Incidence:
<1.0%*
Severity: SEVERE
Onset: EARLY
Vomiting Incidence:
1.1%*
Severity: MILD
Onset: EARLY
Tooth Pain Incidence:
1.1%*
Severity: MILD
Onset: DELAYED
Rhinitis Incidence:
1.6%*
Severity: MILD
Onset: EARLY
Sinus Infection Incidence:
1.7%*
Severity: MILD
Onset: DELAYED
Loose Stools Incidence:
2.7%*
Severity: MILD
Onset: EARLY
Cough Incidence:
3.0%*
Severity: MILD
Onset: DELAYED
Sore Throat Incidence:
5.5%*
Severity: MILD
Onset: DELAYED
Headache Incidence:
6.6%*
Severity: MILD
Onset: EARLY
*This is an approximate aggregated range of reported side effects from clinical studies performed on this drug. Your experience with this drug may be different.
Pregnancy & Lactation Information
FIRST Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

SECOND Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

THIRD Trimester

Class C - Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.

Lactation

Caution - Not enough information is available to rule out harm to infants when this drug is taken by nursing mothers.


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