COLYTE- polyethylene glycol 3350, sodium chloride, potassium chloride, sodium bicarbonate and sodium sulfate anhydrous powder, for solution
Alaven Pharmaceutical LLC
----------
DESCRIPTION
colyte® with flavor packs is a colon lavage preparation provided as water-soluble components for solution. In solution this preparation with one flavor pack delivers the following, in grams per liter.
| Polyethylene glycol 3350 | 60.00 |
| Sodium chloride | 1.46 |
| Potassium chloride | 0.745 |
| Sodium bicarbonate | 1.68 |
| Sodium sulfate | 5.68 |
| Flavor ingredients | 0.851 |
When dissolved in sufficient water to make 1 gallon, the final solution contains 125 mEq/L sodium, 10 mEq/L potassium, 20 mEq/L bicarbonate, 80 mEq/L sulfate, 35 mEq/L chloride and 18 mEq/L polyethylene glycol 3350. The reconstituted solution is isosmotic and has a mildly salty taste. This preparation can be used without the flavor packs and is administered orally or via nasogastric tube.
Each orange flavor pack (3.22 g) contains hypromellose, natural and artifical orange powder, saccharin sodium, colloidal silicon dioxide. Each lemon lime flavor pack (3.22 g) contains, hypromellose, natural and artifical lemon lime powder, Prosweet® Powder Natural, saccharin sodium, colloidal silicon dioxide. Each cherry flavor pack (3.22 g) contains hypromellose, artifical cherry powder, saccharin sodium, colloidal silicon dioxide.
CLINICAL PHARMACOLOGY
colyte® with flavor packs cleanses the bowel by induction of diarrhea. The osmotic activity of polyethylene glycol 3350, in combination with the electrolyte concentration, results in virtually no net absorption or excretion of ions or water. Accordingly, large volumes may be administered without significant changes in fluid and electrolyte balance.
INDICATIONS AND USAGE
colyte® with flavor packs is indicated for bowel cleansing prior to colonoscopy or barium enema X-ray examination.
CONTRAINDICATIONS
colyte® with flavor packs is contraindicated in patients known to be hypersensitive to any of the components. colyte® with flavor packs is contraindicated in patients with ileus, gastrointestinal obstruction, gastric retention, bowel perforation, toxic colitis or toxic megacolon.
WARNINGS
Flavor packs are for use only in combination with the contents of the accompanying 1 gallon container. No other additional ingredients (e.g., flavorings) should be added to the solution. colyte® with flavor packs should be used with caution in patients with severe ulcerative colitis.
PRECAUTIONS
General
Patients with impaired gag reflex, unconscious or semiconscious patients and patients prone to regurgitation or aspiration should be observed during the administration of colyte® with flavor packs, especially if it is administered via nasogastric tube.
If gastrointestinal obstruction or perforation is suspected appropriate studies should be performed to rule out these conditions before administration of colyte® with flavor packs.
Information for Patients
colyte® with flavor packs produces a watery stool which cleanses the bowel prior to examination.
For best results, no solid food should be ingested during the 3 - 4 hour period prior to the initiation of colyte® with flavor packs administration. In no case should solid foods be eaten within 2 hours of drinking colyte® with flavor packs.
The rate of administration is 240 mL (8 fl. oz.) every 10 minutes. Rapid drinking of each portion is preferred rather than drinking small amounts continuously.
The first bowel movement should occur approximately one hour after the start of colyte® with flavor packs administration.
Administration of colyte® with flavor packs should be continued until the watery stool is clear and free of solid matter. This normally requires the consumption of approximately 3-4 liters (3-4 quarts), although more or less may be required in some patients. The unused portion should be discarded.
Drug Interactions
Oral medication administered within one hour of the start of administration of colyte® with flavor packs may be flushed from the gastrointestinal tract and not absorbed.
Carcinogenesis, Mutagenesis, Impairment of Fertility
Studies to evaluate carcinogenic or mutagenic potential or potential to adversely affect male or female fertility have not been performed.
Pregnancy
Category C
Animal reproduction studies have not been conducted with colyte® with flavor packs, and it is not known whether colyte® with flavor packs can affect reproductive capacity or harm the fetus when administered to a pregnant patient. colyte® with flavor packs should be given to a pregnant patient only if clearly needed.
Geriatric Use
Published literature contains isolated reports of serious adverse reactions following the administration of PEG-ELS products in patients over 60 years of age. These adverse events include upper GI bleeding from Mallory-Weiss Tear, esophageal perforation, asystole, sudden dyspnea with pulmonary edema, and "butterfly-like" infiltrate on chest x-ray after vomiting and aspirating PEG.
ADVERSE REACTIONS
Nausea, abdominal fullness and bloating are the most frequent adverse reactions, occurring in up to 50% of patients. Abdominal cramps, vomiting and anal irritation occur less frequently. These adverse reactions are transient. Isolated cases of urticaria, rhinorrhea, dermatitis, and rarely anaphylaxis, angioedema, tongue edema, and face edema have been reported which may represent allergic reactions.
DOSAGE AND ADMINISTRATION
colyte® with flavor packs can be administered orally or by nasogastric tube. Patients should fast at least 3 hours prior to administration. A one hour waiting period after the appearance of clear liquid stool should be allowed prior to examination to complete bowel evacuation. No foods except clear liquids should be permitted prior to examination after colyte® with flavor packs administration.
Oral
The recommended adult oral dose is 240 mL (8 fl. oz.) every 10 minutes (see PRECAUTIONS, Information for Patients). Lavage is complete when fecal discharge is clear. Lavage is usually complete after the ingestion of 3-4 liters (3-4 quarts).
Nasogastric Tube
colyte® with flavor packs is administered at a rate of 20-30 mL per minute (1.2-1.8 L/hour).
Preparation of colyte® with flavor packs Solution
This preparation can be used with or without flavor packs.
- To add flavor, tear open one flavor pack at the indicated marking and pour contents into the bottle BEFORE reconstitution. Discard unused flavor packs.
- SHAKE WELL to incorporate flavoring into powder.
- Add tap water to FILL line. Replace cap tightly and mix or shake well until all ingredients have dissolved. (No other additional ingredients, e.g. flavorings, should be added to the solution.)
Note: If not using flavor packs, omit steps one and two above.
HOW SUPPLIED
colyte® with flavor packs is supplied in 1 gallon bottles with an attached package containing flavor packs. Each 1 gallon bottle contains polyethylene glycol 3350 227.10 g, sodium chloride 5.53 g, potassium chloride 2.82 g, sodium bicarbonate 6.36 g, sodium sulfate (anhydrous) 21.50 g. Each preparation is supplied in powdered form, for oral administration as a solution.
| colyte® with flavor packs | 1 gallon | NDC 68220-133-01 |
Rx only
Manufactured for:
ALAVEN Pharmaceutical LLC
Marietta, GA, USA
For Medical Inquires,
Call toll-free 1-888-317-0001
4011310 Rev. 1E 06/2010 133-0310-02
PRINCIPAL DISPLAY PANEL - Colyte Label
NDC 68220-133-01
Note to pharmacist: Dispense bottle and
all attached flavor packs to patient. Package
insert enclosed. Remove before dispensing.
colyte®
with
Flavor Packs
(peg-3350 & electrolytes for oral solution)
Rx Only
4011310 Rev. 1E 06/2010 133-0310-01
Contents make 1 Gallon (3.785 Liters) of solution
This package contains the following ingredients:
| Polyethylene glycol 3350 | 227.10 grams |
| Sodium chloride | 5.53 grams |
| Potassium chloride | 2.82 grams |
| Sodium bicarbonate | 6.36 grams |
| Sodium sulfate (anhydrous) | 21.50 grams |
When dissolved in sufficient water to make 1 gallon, the final solution contains
125 mEq/L sodium, 10 mEq/L potassium, 20 mEq/L bicarbonate, 80 mEq/L
sulfate, 35 mEq/L chloride and 18 mEq/L polyethylene glycol 3350.
Store powder at 20° to 25°C (68° to 77°F); excursions permitted between
15° to 30°C (59° to 86°F).
KEEP RECONSTITUTED SOLUTION REFRIGERATED.
USE WITHIN 48 HOURS. DISCARD UNUSED PORTION.
APPROXIMATE NET WEIGHT: 263 GRAMS
Filled by net weight, product may settle.
ALAVEN®
PHARMACEUTICAL LLC
1 gallon (3.785 liters)
PRINCIPAL DISPLAY PANEL - 3.22 g Orange Flavor Pack Label
Attention Pharmacist: Dispense all
attached flavor packs to the patient.
orange
flavor pack
FOR USE ONLY IN COMBINATION WITH
THE ACCOMPANYING CONTAINER.
net wt. 3.22 g
| COLYTE
polyethylene glycol 3350, sodium chloride, potassium chloride, sodium bicarbonate, and sodium sulfate anhydrous powder, for solution |
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||
| Labeler - Alaven Pharmaceutical LLC (140210829) |
| Registrant - Schwarz - UCB (006422406) |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
| Schwarz - UCB | 006422406 | ANALYSIS, MANUFACTURE | |