Tuesday, September 13, 2016

PB Hyos Elixir



phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide

Dosage Form: oral elixir
PB Hyos Elixir

DESCRIPTION:


Each 5 mL (teaspoonful) of elixir contains:

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

(WARNING: may be habit forming)

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

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

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

Alcohol not more than 23.8%



INACTIVE INGREDIENTS:


Artificial Grape Flavor, Ethyl Alcohol, FDC Blue #1, FDC Red #40, Glycerin, Purified Water USP, Sodium Saccharin, Sorbitol Solution 70%, and Sucrose.



CLINICAL PHARMACOLOGY:


This drug combination provides peripheral anticholinergic/antispasmodic action and mild sedation.



INDICATIONS AND USAGE:


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.



CONTRAINDICATIONS:


PB Hyos Elixir is contraindicated in patients with known hypersensitivity to any of the ingredients. Phenobarbital is contraindicated in patients with acute intermittent porphyria and in those patients in which phenobarbital produces restlessness and/or excitement.


It is also contraindicated in patients with glaucoma, obstructive uropathy; paralytic ileus; myasthenia gravis; intestinal atony; unstable cardiovascular status in acute hemorrhage; hiatal hernia associated with reflux esophagitis; obstructive disease of the gastrointestinal tract; or severe ulcerative colitis.



WARNINGS:


Heat prostration can occur with belladonna alkaloids in high temperatures.


Diarrhea may be an early symptom of incomplete intestinal obstruction, especially in patients with ileostomy or colostomy. In this instance, treatment with this drug could be harmful.


PB Hyos Elixir may produce drowsiness and blurred vision. The patient should be warned about engaging in hazardous work or activities requiring mental alertness, such as operating a motor vehicle or other machinery.


Phenobarbital may decrease the effect of anticoagulants, and larger doses of the anticoagulant may be needed for optimal effect. When phenobarbital is discontinued, the dose of the anticoagulant may have to be decreased. Phenobarbital may be habit forming and should not be administered to patients who are susceptible to addiction or to those with a history of physical and/or psychological drug dependence.


Barbiturates should be used with caution in patients with hepatic dysfunction.



PRECAUTIONS:


GENERAL: 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.


CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY: Long-term studies in animals have not been performed to evaluate carcinogenic potential.


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


NURSING MOTHERS: 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 PB Hyos Elixir is administered to a nursing woman.



ADVERSE REACTIONS:


Adverse reactions associated with anticholinergics and/or anticonvulsants are: dry mouth; tachycardia; urinary hesitancy and retention; palpitation; blurred vision; prolonged pupil dilation; cycloplegia; increased ocular tension; loss of taste sense; headache; nervousness; drowsiness; weakness; dizziness; insomnia; nausea; vomiting; severe allergic reaction or drug idiosyncrasies, including anaphylaxis, hives and/or other dermal manifestations; decreased sweating; impotence; suppression of lactation; constipation; bloated feeling and musculoskeletal pain. Elderly patients may react with symptoms of excitement, agitation and drowsiness 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.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.



OVERDOSAGE:


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. Call your doctor or local Poison Control Center if overdosage is suspected.



DOSAGE AND ADMINISTRATION:


The dosage of 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: For children age 2 and under, consult a physician for dosage and administration. Children ages 2 and over may be dosed every 4 to 6 hours.




HOW SUPPLIED:


PB Hyos Elixir is a purple colored, grape flavored liquid. 1 Pint (16 fl oz.) bottles NDC 49769-395-16.


Tamper evident by foil seal under cap. Do not use if foil seal is broken or missing.


WARNINGS: KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN. IN CASE OF ACCIDENTAL OVERDOSE, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.


Manufactured for:

Kylemore Pharmaceuticals

Port St. Joe, FL 32456

Rev. 02/10 395-10



PACKAGING:


Below represents the current labeling being used:










PB HYOS 
phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide  elixir










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)49769-395
Route of AdministrationORALDEA Schedule    

















Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENOBARBITAL (PHENOBARBITAL)PHENOBARBITAL16.2 mg  in 5 mL
HYOSCYAMINE SULFATE (HYOSCYAMINE)HYOSCYAMINE SULFATE0.1037 mg  in 5 mL
ATROPINE SULFATE (ATROPINE)ATROPINE SULFATE0.0194 mg  in 5 mL
SCOPOLAMINE HYDROBROMIDE (SCOPOLAMINE)SCOPOLAMINE HYDROBROMIDE0.0065 mg  in 5 mL




















Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
FD&C BLUE NO. 1 
FD&C RED NO. 40 
GLYCERIN 
WATER 
SACCHARIN SODIUM 
SORBITOL 
SUCROSE 


















Product Characteristics
ColorpurpleScore    
ShapeSize
FlavorGRAPEImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
149769-395-16473 mL In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/01/201010/31/2012


Labeler - Kylemore Pharmaceuticals, LLC (831892471)
Revised: 03/2011Kylemore Pharmaceuticals, LLC




More PB Hyos Elixir resources


  • PB Hyos Elixir Side Effects (in more detail)
  • PB Hyos Elixir Dosage
  • PB Hyos Elixir Use in Pregnancy & Breastfeeding
  • PB Hyos Elixir Drug Interactions
  • PB Hyos Elixir Support Group
  • 0 Reviews for PB Hyos - Add your own review/rating


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