FDA records indicate that there are no current recalls for this drug.
Are you a medical professional?
Trending Topics
Prascend Recall
Get an alert when a recall is issued.
Questions & Answers
Side Effects & Adverse Reactions
Do not use in horses intended for human consumption.
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
There is currently no usage information available for this product. We apologize for any inconvenience.
History
There is currently no drug history available for this drug.
Other Information
Prascend Tablets are rectangular light red colored, half-scored tablets containing 1 mg pergolide, as pergolide mesylate. Pergolide mesylate is a synthetic ergot derivative and is a potent dopamine receptor agonist. The chemical name of pergolide mesylate is 8β-[(Methylthio) methyl]-6-propylergoline monomethanesulfonate.
The chemical structure is:
Sources
Prascend Manufacturers
-
Boehringer Ingelheim Vetmedica, Inc.
Prascend | Boehringer Ingelheim Vetmedica, Inc.
Administer orally at a starting dose of 2 mcg/kg once daily. Dosage may be adjusted to effect, not to exceed 4 mcg/kg daily. It has been reported that pergolide tablets may cause eye irritation, an irritating smell, or headache when Prascend Tablets are split or crushed. Prascend Tablets should not be crushed due to the potential for increased human exposure and care should be taken to minimize exposure when splitting tablets.
The tablets are scored and the calculated dosage should be provided to the nearest one-half tablet increment (see Table 1).
Table 1 Dosing Table Dosage Dosage Body weight 2 mcg/kg 4 mcg/kg136 - 340 kg
(300 - 749 lb)
0.5 tablet 1 tablet341 - 567 kg
750 - 1,249 lb)
1 tablet 2 tablets568 - 795 kg
(1,250 - 1,749 lb)
1.5 tablets 3 tablets796 - 1,022 kg
(1,750 - 2,249 lb)
2 tablets 4 tabletsDosing should be titrated according to individual response to therapy to achieve the lowest effective dose. Dose titration is based on improvement in clinical signs associated with Pituitary Pars Intermedia Dysfunction (PPID) and/or improvement or normalization of endocrine tests (for example, dexamethasone suppression test or endogenous ACTH test). If signs of dose intolerance develop, the dose should be decreased by half for 3 to 5 days and then titrated back up in 2 mcg/kg increments every 2 weeks until the desired effect is achieved.
Login To Your Free Account