What is Levsin SL and how is it used?
Levsin SL is a prescription medicine used to treat the symptoms of Gastrointestinal Disorders, Hypermotility of Lower Urinary Tract, Peptic Ulcer Disease, and Irritable Bowel Syndrome (IBS). Levsin SL may be used alone or with other medications.
Levsin SL belongs to a class of drugs called Anticholinergic Agents.
It is not known if Levsin SL is safe and effective in children younger than 2 years of age.
What are the possible side effects of Levsin SL?
Levsin SL may cause serious side effects including:
- difficulty breathing,
- swelling of your face, lips, tongue, or throat,
- unusual thoughts or behavior,
- memory problems,
- slurred speech,
- problems with balance or muscle movement,
- diarrhea, and
- pounding heartbeats or fluttering in your chest
Get medical help right away, if you have any of the symptoms listed above.
The most common side effects of Levsin SL include:
- decreased sweating,
- decreased urination,
- blurred vision,
- dry mouth,
- decreased sense of taste,
- stomach pain,
- sleep problems (insomnia),
- loss of interest in sex, and
- trouble having an orgasm
Tell the doctor if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of Levsin SL. For more information, ask your doctor or pharmacist.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Levsin®/SL tablets (hyoscyamine sulfate tablets USP) contain 0.125 mg hyoscyamine sulfate formulated for sublingual administration. However, the tablets may be chewed or taken orally.
Levsin®/SL (hyoscyamine sulfate tablets) is one of the principal anticholinergic/antispasmodic components of belladonna alkaloids. The empirical formula is (C17H23NO3)2•H2SO4•2H2O and the molecular weight is 712.85. Chemically, it is benzeneacetic acid, ~-(hydroxymethyl)-,8-methyl-8-azabicyclo [3.2.1.] oct-3-yl ester, [3(S)-endo]-, sulfate (2:1), dihydrate with the following structure:
Each tablet also contains as inactive ingredients: FD&C blue #1, lactose monohydrate, magnesium stearate, mannitol, starch and stearic acid.
Levsin®/SL (hyoscyamine sulfate tablets) is effective as adjunctive therapy in the treatment of peptic ulcer. It can also be used to control gastric secretion, visceral spasm and hypermotility in spastic colitis, spastic bladder, cystitis, pylorospasm, and associated abdominal cramps. May be used in functional intestinal disorders to reduce symptoms such as those seen in mild dysenteries, diverticulitis, and acute enterocolitis. For use as adjunctive therapy in the treatment of irritable bowel syndrome (irritable colon, spastic colon, mucous colitis) and functional gastrointestinal disorders. Also used as adjunctive therapy in the treatment of neurogenic bladder and neurogenic bowel disturbances (including the splenic flexure syndrome and neurogenic colon). Also used in the treatment of infant colic (elixir and drops). Levsin®/SL (hyoscyamine sulfate tablets) is indicated along with morphine or other narcotics in symptomatic relief of biliary and renal colic; as a “drying agent” in the relief of symptoms of acute rhinitis; in the therapy of parkinsonism to reduce rigidity and tremors and to control associated sialorrhea and hyperhidrosis. May be used in the therapy of poisoning by anticholinesterase agents.
DOSAGE AND ADMINISTRATION
Dosage may be adjusted according to the conditions and severity of symptoms. The tablets may be taken sublingually, orally or chewed.
Adults and pediatric patients 12 years of age and older
1 to 2 tablets every four hours or as needed. Do not exceed 12 tablets in 24 hours.
Pediatric patients 2 to under 12 years of age: ½ to 1 tablet every four hours or as needed. Do not exceed 6 tablets in 24 hours.
Levsin®/SL tablets (hyoscyamine sulfate tablets USP) 0.125 mg are round, blue colored tablets that are imprinted with “AP” on one side and “113” on the other.
Bottles of 100 tablets NDC 68220-113-10
Bottles of 500 tablets NDC 68220-113-50
Store at controlled room temperature 20°- 25°C (68° - 77°F); excursions permitted to15°- 30°C (59°- 86°F). Please refer to current USP.
Dispense in tight, light-resistant containers as defined in USP/NF with a child-resistant closure.
KEEP OUT OF REACH OF CHILDREN
Also available as:
|Levsin®||Dosage Strength||Package Size||NDC|
|Injection||0.5mg/mL||Box of 5-1mL||0091-1536-05|
|Levbid® extended-release tablets||0.375mg||100||68220-115-10|
Manufactured for: Alaven Pharmaceutical LLC, Marietta, GA 30067. Address medical inquiries to: Alaven Pharmaceutical LLC, 2260 Northwest Parkway, Suite A, Marietta, GA 30067 Or call toll free 1-888-317-0001. Rev: 02/08.
All of the following adverse reactions have been reported with hyoscyamine sulfate. Adverse reactions may include dryness of the mouth; urinary hesitancy and retention; blurred vision; tachycardia; palpitations; mydriasis; increased ocular tension; loss of taste; headache; nervousness; drowsiness; weakness; fatigue; dizziness; insomnia; nausea; vomiting; impotence; constipation; bloated feeling; abdominal pain; diarrhea; allergic reactions or drug idiosyncrasies; urticaria and other dermal manifestations; ataxia; speech disturbance; some degree of mental confusion and/or excitement (especially in elderly persons); short-term memory loss; hallucinations; and decreased sweating.
Additive adverse effects resulting from cholinergic blockade may occur when Levsin®/SL (hyoscyamine sulfate tablets) is administered concomitantly with other antimuscarinics, amantadine, haloperidol, phenothiazines, monoamine oxidase (MAO) inhibitors, tricyclic antidepressants or some antihistamines.
Antacids may interfere with the absorption of Levsin®/SL (hyoscyamine sulfate tablets) . Administer Levsin®/SL (hyoscyamine sulfate tablets) before meals; antacids after meals.
In the presence of high environmental temperature, heat prostration can occur with drug use (fever and heat stroke 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. Like other anticholinergic agents, Levsin®/SL (hyoscyamine sulfate tablets) may produce drowsiness, dizziness or blurred vision. In this event, the patient should be warned not to engage in activities requiring mental alertness such as operating a motor vehicle or other machinery or to perform hazardous work while taking this drug.
Psychosis has been reported in sensitive individuals given anticholinergic drugs including hyoscyamine sulfate. CNS signs and symptoms include confusion, disorientation, short-term memory loss, hallucinations, dysarthria, ataxia, euphoria, anxiety, fatigue, insomnia, agitation and mannerisms, and inappropriate affect. These CNS signs and symptoms usually resolve within 12 to 48 hours after discontinuation of the drug.
Use with caution in patients with: autonomic neuropathy, hyperthyroidism, coronary heart disease, congestive heart failure, cardiac arrhythmias, hypertension, and renal disease. Investigate any tachycardia before giving any anticholinergic drug since they may increase the heart rate. Use with caution in patients with hiatal hernia associated with reflux esophagitis.
Carcinogenesis, Mutagenesis, Impairment of Fertility
No long-term studies in animals have been performed to determine the carcinogenic, mutagenic or impairment of fertility potential of Levsin®/SL; however, 40 years of marketing experience with hyoscyamine sulfate shows no demonstrable evidence of a problem.
Pregnancy-Pregnancy Category C
Animal reproduction studies have not been conducted with Levsin®/SL (hyoscyamine sulfate tablets) . It is also not known whether Levsin®/SL (hyoscyamine sulfate tablets) can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Levsin®/SL (hyoscyamine sulfate tablets) should be given to a pregnant woman only if clearly needed.
Levsin®/SL (hyoscyamine sulfate tablets) is excreted in human milk. Caution should be exercised when Levsin®/SL (hyoscyamine sulfate tablets) is administered to a nursing woman.
Reported clinical experience has not identified differences in safety between patients aged 65 and over and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.
This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.
Measures to be taken are immediate lavage of the stomach and injection of physostigmine 0.5 to 2 mg intravenously and repeated as necessary up to a total of 5 mg. Fever may be treated symptomatically (tepid water sponge baths, hypothermic blanket). Excitement to a degree which demands attention may be managed with sodium thiopental 2% solution given slowly intravenously or chloral hydrate (100-200 mL of a 2% solution) by rectal infusion. In the event of progression of the curare-like effect to paralysis of the respiratory muscles, artificial respiration should be instituted and maintained until effective respiratory action returns.
In rats, the LD50 for hyoscyamine is 375 mg/kg. Levsin®/SL (hyoscyamine sulfate tablets) is dialyzable.
Glaucoma; obstructive uropathy (for example, bladder neck obstruction due to prostatic hypertrophy); obstructive disease of the gastrointestinal tract (as in achalasia, pyloroduodenal stenosis): paralytic ileus, intestinal atony of elderly or debilitated patients; unstable cardiovascular status in acute hemorrhage; severe ulcerative colitis; toxic megacolon complicating ulcerative colitis; myasthenia gravis.
Levsin®/SL (hyoscyamine sulfate tablets) inhibits specifically the actions of acetylcholine on structures innervated by postganglionic cholinergic nerves and on smooth muscles that respond to acetylcholine but lack cholinergic innervation. These peripheral cholinergic receptors are present in the autonomic effector cells of the smooth muscle, cardiac muscle, the sinoatrial node, the atrioventricular node, and the exocrine glands. At therapeutic doses, it is completely devoid of any action on autonomic ganglia. Levsin®/SL (hyoscyamine sulfate tablets) inhibits gastrointestinal propulsive motility and decreases gastric acid secretion. Levsin®/SL (hyoscyamine sulfate tablets) also controls excessive pharyngeal, tracheal and bronchial secretions.
Levsin®/SL (hyoscyamine sulfate tablets) is absorbed totally and completely by sublingual administration as well as oral administration. Once absorbed, Levsin®/SL (hyoscyamine sulfate tablets) disappears rapidly from the blood and is distributed throughout the entire body. The half-life of Levsin®/SL (hyoscyamine sulfate tablets) is 2 to 3½ hours. Levsin®/SL (hyoscyamine sulfate tablets) is partly hydrolyzed to tropic acid and tropine but the majority of the drug is excreted in the urine unchanged within the first 12 hours. Only traces of this drug are found in breast milk. Levsin®/SL (hyoscyamine sulfate tablets) passes the blood brain barrier and the placental barrier. The tablets can be taken orally with the same pharmacological effects occurring; however, the effects may not occur as rapidly as with sublingual administration.
Like other anticholinergic agents, Levsin®/SL (hyoscyamine sulfate tablets) may produce drowsiness, dizziness, or blurred vision. In this event, the patient should be warned not to engage in activities requiring mental alertness such as operating a motor vehicle or other machinery or to perform hazardous work while taking this drug.
Use of Levsin®/SL (hyoscyamine sulfate tablets) may decrease sweating resulting in heat prostration, fever or heat stroke; febrile patients or those who may be exposed to elevated environmental temperatures should use caution.
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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