Viokace Oral Tablet 10440-39150-39150U Drug Medication Dosage Information
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Viokace: Oral tablet (10440-39150-39150U)

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Viokace 10 Tablet
Actavis- US Brands formerly Aptalis Pharma, a wholly owned subsidiary of Forest, Formerly Axcan Pharma US, Inc.
Pill Identification: VIO9111  |  9111

What is this Medicine?

PANCRELIPASE (pan cre LI pase) helps to improve digestion of food by replacing digestive enzymes. This medicine is used to treat health conditions that cause your body to produce less of these enzymes.

In-Depth Information

Viokace 10 Tablet

NDC: 589140112
  • Prescription Required
  • Not a Controlled Drug
    (CSA Schedule)
  • FDA Approved




FDA approved for the following conditions:
Pancreatectomy, Cystic Fibrosis, Pancreatic Insufficiency

Sometimes used for but not FDA approved for the following conditions:
Feeding Tube Occlusion

Storage Information
Avoid exposure to heat
Store in original container
Store in a dry place
Protect from moisture
Store between 68 to 77 degrees F; brief excursions permitted to 104 degrees F
Viokace 10 Tablet
Drug Image file DrugItem_15931.JPG
Actavis- US Brands formerly Aptalis Pharma, a wholly owned subsidiary of Forest, Formerly Axcan Pharma US, Inc.
Pill Identification: VIO9111  |  9111
Shape: round
Color: tan

Reported Side Effects for Viokace 10 Tablet

Skin Rash Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Rash With Pustules Incidence:
<1.0%*
Severity: MILD
Onset: EARLY
Breathing Difficulties Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Anaphylactoid Reactions Incidence:
<1.0%*
Severity: SEVERE
Onset: RAPID
Hives Incidence:
<1.0%*
Severity: MILD
Onset: RAPID
Itching Incidence:
<1.0%*
Severity: MILD
Onset: RAPID
Headache Incidence:
3.0-15.0%*
Severity: MILD
Onset: EARLY
Infection Incidence:
3.0-11.0%*
Severity: MILD
Onset: DELAYED
Gas Incidence:
3.0-9.0%*
Severity: MILD
Onset: EARLY
Stomach Pain Incidence:
3.0-18.0%*
Severity: MILD
Onset: EARLY
Lightheadedness Incidence:
4.0-6.0%*
Severity: MILD
Onset: EARLY
Cough Incidence:
4.0-10.0%*
Severity: MILD
Onset: DELAYED
Vomiting Incidence:
6.0%*
Severity: MILD
Onset: EARLY
Upset Stomach Incidence:
10.0%*
Severity: MILD
Onset: EARLY
Loose Stools Incidence:
10.0%*
Severity: MILD
Onset: EARLY
Ear Pain Incidence:
11.0%*
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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