Kapvay Oral Tablet, Extended Release 0.1Mg Drug Medication Dosage Information
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Kapvay: Oral tablet, extended release (0.1mg)

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Drug Image file DrugItem_18196.JPG
Kapvay 0.1 mg ER Tablet
Concordia Pharmaceuticals Inc.
Pill Identification: 651 

What is this Medicine?

CLONIDINE (KLOE ni deen) is used to treat attention-deficit hyperactivity disorder (ADHD).

CVS Pharmacy Patient Statistics for Kapvay: Oral tablet, extended release(0.1mg)
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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Kapvay 0.1mg Extended-Release Tablet

NDC: 592120658
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved





Storage Information
Store at controlled room temperature (between 68 and 77 degrees F)
Kapvay 0.1mg Extended-Release Tablet
Drug Image file DrugItem_18196.JPG
Concordia Pharmaceuticals Inc.
Pill Identification: 651 
Shape: round
Color: white
Daily Life Interactions for Kapvay 0.1mg Extended-Release Tablet

Elements of your daily lifestyle may have an effect on the medications you are taking. Drug interactions can result in unwanted side effects, reduce the effectiveness of your medicine or possibly increase the action of a particular medicine.

Major Lifestyle Interaction
Alcohol and Kapvay 0.1mg Extended-Release Tablet(Clonidine Hydrochloride)
Alcohol and Clonidine(Clonidine Hydrochloride)
t is best to limit or avoid alcohol intake if you take Clonidine. Alcohol-containing beverages may increase the side effects of Clonidine, which may cause sedation or lower the blood pressure. If the blood pressure drops too low, you may become dizzy or feel faint. Do not stand or sit up too quickly. Contact your prescriber if you have dizziness which does not go away. Do not drive or operate machinery or perform other hazardous tasks until you know how Clonidine affects you.
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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