Me-PB-Hyos description, usages, side effects, indications, overdosage, supplying and lots more!

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Me-PB-Hyos

Method Pharmaceuticals, Inc.

Me-PB-Hyos Elixir




FULL PRESCRIBING INFORMATION

Me-PB-Hyos Elixir
Rx only
Me-PB-Hyos
Rev. 04/2014

Me-PB-Hyos Elixir - Grape:

Each 5 mL (teaspoonful) of elixir (alcohol not more than 23.8%) contains:

Phenobarbital, USP ................................................... 16.2 mg

Hyoscyamine Sulfate, USP ................................... 0.1037 mg

Atropine Sulfate, USP ........................................... 0.0194 mg

Scopolamine Hydrobromide, USP ......................... 0.0065 mg

Ethyl Alcohol, FD&C Blue #2, FD&C Red #40, Artificial Grape Flavor, Glycerin, Purified Water, Saccharin Sodium, Sorbitol, Sucrose.

This drug combination provides natural belladonna alkaloids in a specific, fixed ratio combined with phenobarbital to provide peripheral anticholinergic/ antispasmodic action and mild sedation.

Based on a review of this drug by the National Academy of Sciences-National Research Council and/or other information, FDA has classified the following indications as “possibly” effective: For use as adjunctive therapy in the treatment of irritable bowel syndrome (irritable colon, spastic colon, mucous colitis) and acute enterocolitis. May also be useful as adjunctive therapy in the treatment of duodenal ulcer. IT HAS NOT BEEN SHOWN CONCLUSIVELY WHETHER ANTICHOLINERGIC/ ANTISPASMODIC DRUGS AID IN THE HEALING OF A DUODENAL ULCER, DECREASE THE RATE OF RECURRENCES OR PREVENT COMPLICATIONS.

Glaucoma, obstructive uropathy (for example, bladder neck obstruction due to prostatic hypertrophy); obstructive disease of the gastrointestinal tract (as in achalasia, pyloroduodenal stenosis, etc.); paralytic ileus, intestinal atony of the elderly or debilitated patient; unstable cardiovascular status in acute hemorrhage; severe ulcerative colitis especially if complicated by toxic megacolon; myasthenia gravis; hiatal hernia associated with reflux esophagitis. Me-PB-Hyos Elixir is contraindicated in patients with known hypersensitivity to any of the ingredients. Phenobarbital is contraindicated in acute intermittent porphyria and in those patients in whom phenobarbital produces restlessness and/or excitement.

In the presence of a high environmental temperature, heat prostration can occur with belladonna alkaloids (fever and heatstroke due to decreased sweating). Diarrhea may be an early symptom of incomplete intestinal obstruction, especially in patients with ileostomy or colostomy. In this instance, treatment with this drug would be inappropriate and possibly harmful.

Me-PB-Hyos Elixir may produce drowsiness or blurred vision. The patient should be warned, should these occur, not to engage in activities requiring mental alertness, such as operating a motor vehicle or other machinery, and not to perform hazardous work. Phenobarbital may decrease the effect of anticoagulants, and necessitate larger doses of the anticoagulant for optimal effect. When the phenobarbital is discontinued, the dose of the anticoagulant may have to be decreased. Phenobarbital may be habit forming and should not be administered to individuals known to be addiction prone or to those with a history of physical and/or psychological dependence upon drugs. Since barbiturates are metabolized in the liver, they should be used with caution and initial doses should be small in patients with hepatic dysfunction.

Use with caution in patients with: autonomic neuropathy, hepatic or renal disease, hyperthyroidism, coronary heart disease, congestive heart failure, cardiac arrhythmias, tachycardia, and hypertension. Belladonna alkaloids may produce a delay in gastric emptying (antral stasis) which would complicate the management of gastric ulcer. Do not rely on the use of the drug in the presence of complication of biliary tract disease. Theoretically, with overdosage, a curare-like action may occur.

Long-term studies in animals have not been performed to evaluate carcinogenic potential.

PREGNANCY CATEGORY C

Animal reproduction studies have not been conducted with Me-PB-Hyos Elixir . It is not known whether Me-PB-Hyos Elixir can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Me-PB-Hyos Elixir should be given to a pregnant woman only if clearly needed.

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Me-PB-Hyos Elixir is administered to a nursing woman.

Adverse reactions may include xerostomia; urinary hesitancy and retention; blurred vision; tachycardia; palpitation; mydriasis; cycloplegia; increased ocular tension; loss of taste sense; headache; nervousness; drowsiness; weakness; dizziness; insomnia; nausea; vomiting; impotence; suppression of lactation; constipation; bloated feeling; musculoskeletal pain; severe allergic reaction or drug idiosyncrasies, including anaphylaxis, urticaria and other dermal manifestations; and decreased sweating. Elderly patients may react with symptoms of excitement, agitation, drowsiness, and other untoward manifestations to even small doses of the drug. Phenobarbital may produce excitement in some patients, rather than a sedative effect. In patients habituated to barbiturates, abrupt withdrawal may produce delirium or convulsions.

Adverse Events:

To report an adverse event, please contact Method Pharmaceuticals Customer Service at 1-877-250-3427.

The signs and symptoms of overdose are headache, nausea, vomiting, blurred vision, dilated pupils, hot and dry skin, dizziness, dryness of the mouth, difficulty in swallowing, and CNS stimulation. Treatment should consist of gastric lavage, emetics, and activated charcoal. If indicated, parenteral cholinergic agents such as physostigmine or bethanechol chloride, should be used.

The dosage of Me-PB-Hyos Elixir should be adjusted to the needs of the individual patient to assure symptomatic control with a minimum of adverse effects.

Adults: One or two teaspoonfuls of elixir three or four times a day according to conditions and severity of symptoms.

Pediatric patients: may be dosed every 4 to 6 hours.

Starting Dosage
Body weight             q4h q6h
10 lb. (4.5 kg)       0.5 mL 0.75 mL
20 lb. (9.1 kg)             1.0 mL 1.5 mL
30 lb. (13.6 kg)       1.5 mL 2.0 mL
50 lb. (22.7 kg)       1/2 tsp 3/4 tsp
75 lb. (34 kg)             3/4 tsp 1 tsp
100 lb. (45.4 kg)       1 tsp 1 1/2 tsp

Me-PB-Hyos Elixir is a purple colored, grape flavored liquid.

1 Pint (473 mL) bottles - NDC 58657-420-16.

Store at controlled room temperature, 15-30°C (59-86°F). Protect from light and moisture.

Dispense in a tight, light-resistant container as defined in the USP using a child-resistant closure. Use safety closures when dispensing this product unless otherwise directed by a physician or requested by purchaser.

Manufactured For:
Method Pharmaceuticals, LLC
Arlington, TX 76006

Rev. 04/2014

NDC 58657-420-16
Me- PB - Hyos
Elixir
grape flavored
1 PINT

Me-PB-Hyos

Me-PB-Hyos

Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide ELIXIR

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:58657-420
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PHENOBARBITAL PHENOBARBITAL 16.2 mg
HYOSCYAMINE SULFATE HYOSCYAMINE 0.1037 mg
atropine sulfate ATROPINE 0.0194 mg
SCOPOLAMINE HYDROBROMIDE SCOPOLAMINE 0.0065 mg

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
FD&C BLUE NO. 2
FD&C RED NO. 40
GLYCERIN
water
saccharin sodium
sorbitol
SUCROSE

Product Characteristics

Color
PURPLE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58657-420-16 473 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2014-06-01


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