Lodosyn

LODOSYN (Carbidopa) tablets contain 25 mg of carbidopa. Inactive ingredients are cellulose, FD&C Yellow 6, magnesium stearate and starch.

Tablet content is expressed in terms of anhydrous carbidopa which has a molecular weight of 226.3.

CLINICAL PHARMACOLOGY

Parkinson's disease is a progressive, neurodegenerative disorder of the extrapyramidal nervous system affecting the mobility and control of the skeletal muscular system. Its characteristic features include resting tremor, rigidity, and bradykinetic movements. Symptomatic treatments, such as levodopa therapies, may permit the patient better mobility.

Mechanism of Action

Current evidence indicates that symptoms of Parkinson's disease are related to depletion of dopamine in the corpus striatum. Administration of dopamine is ineffective in the treatment of Parkinson's disease apparently because it does not cross the blood-brain barrier. However, levodopa, the metabolic precursor of dopamine, does cross the blood-brain barrier, and presumably is converted to dopamine in the brain. This is thought to be the mechanism whereby levodopa relieves symptoms of Parkinson's disease.

Pharmacodynamics

When levodopa is administered orally it is rapidly decarboxylated to dopamine in extracerebral tissues so that only a small portion of a given dose is transported unchanged to the central nervous system. For this reason, large doses of levodopa are required for adequate therapeutic effect and these may often be accompanied by nausea and other adverse reactions, some of which are attributable to dopamine formed in extracerebral tissues.

The incidence of levodopa-induced nausea and vomiting is less when LODOSYN is used with levodopa than when levodopa is used without LODOSYN. In many patients this reduction in nausea and vomiting will permit more rapid dosage titration.

Carbidopa inhibits decarboxylation of peripheral levodopa. Carbidopa has not been demonstrated to have any overt pharmacodynamic actions in the recommended doses. It does not appear to cross the blood-brain barrier readily and does not affect the metabolism of levodopa within the central nervous system at doses of carbidopa that are recommended for maximum effective inhibition of peripheral decarboxylation of levodopa.

Since its decarboxylase-inhibiting activity is limited primarily to extracerebral tissues, administration of carbidopa with levodopa makes more levodopa available for transport to the brain. However, since levodopa and carbidopa compete with certain amino acids for transport across the gut wall, the absorption of levodopa and carbidopa may be impaired in some patients on a high protein diet.

Pharmacokinetics

Carbidopa reduces the amount of levodopa required to produce a given response by about 75% and, when administered with levodopa, increases both plasma levels and the plasma half-life of levodopa, and decreases plasma and urinary dopamine and homovanillic acid.

In clinical pharmacologic studies, simultaneous administration of separate tablets of carbidopa and levodopa produced greater urinary excretion of levodopa in proportion to the excretion of dopamine when compared to the two drugs administered at separate times.

Supplemental pyridoxine (vitamin B₆) can be given to patients when they are receiving carbidopa and levodopa concomitantly or the fixed combination carbidopa-levodopa or carbidopa-levodopa extended release. Previous reports in the medical literature cautioned that high doses of vitamin B₆ should not be taken by patients on levodopa therapy alone because exogenously administered pyridoxine would enhance the metabolism of levodopa to dopamine. The introduction of carbidopa to levodopa therapy, which inhibits the peripheral decarboxylation of levodopa to dopamine, counteracts the metabolic-enhancing effect of pyridoxine.

Carbidopa is combined with levodopa in carbidopa-levodopa and carbidopa-levodopa

extended release tablets.

LODOSYN INDICATIONS AND USAGE

LODOSYN is indicated for use with carbidopa-levodopa or with levodopa in the treatment of

the symptoms of idiopathic Parkinson’s disease (paralysis agitans), postencephalitic parkinsonism, and symptomatic parkinsonism, which may follow injury to the nervous system

by carbon monoxide intoxication and/or manganese intoxication.

LODOSYN is for use with carbidopa-levodopa in patients for whom the dosage of

carbidopa-levodopa provides less than adequate daily dosage (usually 70 mg daily) of

carbidopa.

LODOSYN is for use with levodopa in the occasional patient whose dosage requirement of

carbidopa and levodopa necessitates separate titration of each medication

LODOSYN is used with carbidopa-levodopa or with levodopa to permit the administration

of lower doses of levodopa with reduced nausea and vomiting, more rapid dosage titration,

and with a somewhat smoother response. However, patients with markedly irregular (“on-off”)

responses to levodopa have not been shown to benefit from the addition of carbidopa.

Since carbidopa prevents the reversal of levodopa effects caused by pyridoxine, supplemental

pyridoxine (vitamin B6), can be given to patients when they are receiving carbidopa and

levodopa concomitantly or as carbidopa-levodopa.

Although the administration of LODOSYN permits control of parkinsonism and Parkinson’s

disease with much lower doses of levodopa, there is no conclusive evidence at present that this

is beneficial other than in reducing nausea and vomiting, permitting more rapid titration, and providing a somewhat smoother response to levodopa.

Certain patients who responded poorly to levodopa alone have improved when carbidopa and

levodopa were given concurrently. This was most likely due to decreased peripheral decarboxylation of levodopa rather than to a primary effect of carbidopa on the peripheral

nervous system. Carbidopa has not been shown to enhance the intrinsic efficacy of levodopa.

In deciding whether to give LODOSYN with carbidopa-levodopa or with levodopa to patients who have nausea and/or vomiting, the physician should be aware that, while many patients may be expected to improve, some may not. Since one cannot predict which patients are likely to improve, this can only be determined by a trial of therapy. It should be further noted that in controlled trials comparing carbidopa and levodopa with levodopa alone, about half the patients with nausea and/or vomiting on levodopa alone improved spontaneously despite being retained on the same dose of levodopa during the controlled portion of the trial.

LODOSYN CONTRAINDICATIONS

LODOSYN is contraindicated in patients with known hypersensitivity to any component of this drug.

Nonselective monoamine oxidase (MAO) inhibitors are contraindicated for use with levodopa or carbidopa-levodopa combination products with or without LODOSYN. These inhibitors must be discontinued at least two weeks prior to initiating therapy with levodopa. Carbidopa-levodopa or levodopa may be administered concomitantly with the manufacturer’s recommended dose of an MAO inhibitor with selectivity for MAO type B (e.g., selegiline HCl) (see PRECAUTIONS, Drug Interactions ).

Levodopa or carbidopa-levodopa products, with or without LODOSYN, are contraindicated in patients with narrow-angle glaucoma.

WARNINGS

LODOSYN (Carbidopa) has no antiparkinsonian effect when given alone. It is indicated

for use with carbidopa-levodopa or levodopa. LODOSYN (Carbidopa) does not decrease

adverse reactions due to central effects of levodopa.

When LODOSYN (Carbidopa) is to be given to carbidopa-naive patients who are being treated with levodopa alone, the two drugs should be given at the same time. At least twelve hours should elapse between the last dose of levodopa and initiation of therapy with LODOSYN (Carbidopa) and levodopa in combination. Start with no more than one-fifth (20%) to one-fourth (25%) of the previous daily dosage of levodopa when given without LODOSYN (Carbidopa). See the DOSAGE AND ADMINISTRATION section before initiating therapy.

The addition of LODOSYN with levodopa or carbidopa-levodopa reduces the peripheral

effects (nausea, vomiting) due to decarboxylation of levodopa; however, LODOSYN does

not decrease the adverse reactions due to the central effects of levodopa. Because LODOSYN permits more levodopa to reach the brain and more dopamine to be formed,

certain adverse central nervous system (CNS) effects, e.g., dyskinesias (involuntary

movements), may occur at lower dosages and sooner with levodopa in combination with

LODOSYN than with levodopa alone.

Falling Asleep During Activities of Daily Living and Somnolence

Patients taking carbidopa-levodopa products alone or with other dopaminergic drugs have

reported suddenly falling asleep without prior warning of sleepiness while engaged in activities

of daily living (includes operation of motor vehicles). Some of these episodes resulted in

automobile accidents. Although many of these patients reported somnolence while on

dopaminergic medications, some did perceive that they had no warning signs, such as excessive

drowsiness, and believed that they were alert immediately prior to the event. Some patients

reported these events one year after the initiation of treatment.

Falling asleep while engaged in activities of daily living usually occurs in patients experiencing

pre-existing somnolence, although some patients may not give such a history. For this reason,

prescribers should continually reassess patients for drowsiness or sleepiness especially since

some of the events occur after the start of treatment. Prescribers should be aware that patients

may not acknowledge drowsiness or sleepiness until directly questioned about drowsiness or

sleepiness during specific activities. Patients who have already experienced somnolence or an

episode of sudden sleep onset should not participate in these activities during treatment with

LODOSYN when taking it with other carbidopa-levodopa products.

Before initiating treatment with LODOSYN, advise patients about the potential to develop

drowsiness and ask specifically about factors that may increase the risk for somnolence with

LODOSYN such as the use of concomitant sedating medications and the presence of sleep

disorders. Consider discontinuing LODOSYN in patients who report significant daytime

sleepiness or episodes of falling asleep during activities that require active participation (e.g.,

conversations, eating, etc.). If treatment with LODOSYN continues, patients should be advised

not to drive and to avoid other potentially dangerous activities that might result in harm if the

patients become somnolent. There is insufficient information to establish that dose reduction

will eliminate episodes of falling asleep while engaged in activities of daily living.

As with levodopa alone there is a possibility of upper gastrointestinal hemorrhage in patients with a history of peptic ulcer.

Hyperpyrexia and Confusion

Sporadic cases of a symptom complex resembling neuroleptic malignant syndrome (NMS) have

been reported in association with dose reductions or withdrawal of certain antiparkinsonian

agents such as levodopa, carbidopa-levodopa, or carbidopa-levodopa extended-release. Therefore, patients should be observed carefully when the dosage of levodopa or arbidopalevodopa is reduced abruptly or discontinued, especially if the patient is receiving

neuroleptics.

NMS is an uncommon but life-threatening syndrome characterized by fever or hyperthermia.

Neurological findings, including muscle rigidity, involuntary movements, altered

consciousness, mental status changes; other disturbances, such as autonomic dysfunction,

tachycardia, tachypnea, sweating, hyper- or hypotension; laboratory findings, such as creatine phosphokinase elevation, leukocytosis, myoglobinuria, and increased serum myoglobin, have been reported.

The early diagnosis of this condition is important for the appropriate management of these

patients. Considering NMS as a possible diagnosis and ruling out other acute illnesses

(e.g., pneumonia, systemic infection, etc.) is essential. This may be especially complex if the

clinical presentation includes both serious medical illness and untreated or inadequately treated

extrapyramidal signs and symptoms (EPS). Other important considerations in the differential diagnosis include central anticholinergic toxicity, heat stroke, drug fever, and primary central

nervous system (CNS) pathology.

The management of NMS should include: 1) intensive symptomatic treatment and medical

monitoring and 2) treatment of any concomitant serious medical problems for which specific

treatments are available. Dopamine agonists, such as bromocriptine, and muscle relaxants,

such as dantrolene, are often used in the treatment of NMS; however, their effectiveness has

not been demonstrated in controlled studies.

PRECAUTIONS

General

As with levodopa alone, periodic evaluations of hepatic, hematopoietic, cardiovascular, and

renal function are recommended during extended concomitant therapy with LODOSYN and

levodopa, or with LODOSYN and carbidopa-levodopa or any combination of these drugs.

Postmarketing reports suggest that patients treated with anti-Parkinson medications can

experience intense urges to gamble, increased sexual urges, intense urges to spend money

uncontrollably, binge eating, and other intense urges. Patients may be unable to control these

urges while taking one or more of the medications that are used for the treatment of Parkinson’s

disease and that increase central dopaminergic tone, including Lodosyn taken with levodopa and

carbidopa. In some cases, although not all, these urges were reported to have stopped when the

dose of anti-Parkinson medications was reduced or discontinued. Because patients may not

recognize these behaviors as abnormal it is important for prescribers to specifically ask patients

or their caregivers about the development of new or increased gambling urges, sexual urges,

uncontrolled spending or other urges while being treated with Lodosyn. Physicians should

consider dose reduction or stopping Lodosyn or levodopa if a patient develops such urges while

taking Lodosyn with carbidopa/levodopa.

Hallucinations and psychotic like behavior have been reported with dopaminergic medications.

In general, hallucinations present shortly after the initiation of therapy and may be responsive to

dose reduction in levodopa. Hallucinations may be accompanied by confusion and to a lesser

extent sleep disorder (insomnia) and excessive dreaming. LODOSYN when taken with

carbidopa-levodopa may have similar effects on thinking and behavior. This abnormal thinking

and behavior may present with one or more symptoms, including paranoid ideation, delusions,

hallucinations, confusion, psychotic-like behavior, disorientation, aggressive behavior,

agitation, and delirium.

Ordinarily, patients with a major psychotic disorder should not be treated with LODOSYN and

carbidopa-levodopa, because of the risk of exacerbating psychosis. In addition, certain medications used to treat psychosis may exacerbate the symptoms of Parkinson’s disease and

may decrease the effectiveness of LODOSYN.

LODOSYN (Carbidopa) may potentiate the dopaminergic side effects of levodopa and may

cause or exacerbate preexisting dyskinesia.

Patients treated with LODOSYN and carbidopa-levodopa should be observed carefully for the

development of depression with concomitant suicidal tendencies.

Epidemiological studies have shown that patients with Parkinson’s disease have a higher risk

(2-to approximately 6-fold higher) of developing melanoma than the general population.

Whether the observed increased risk was due to Parkinson’s disease or other factors, such as drugs used to treat Parkinson’s disease, is unclear.

For the reasons stated above, patients and providers are advised to monitor for melanomas

frequently and on a regular basis when using LODOSYN tablets for Parkinson’s disease.

Ideally, periodic skin examinations should be performed by appropriately qualified individuals

(e.g., dermatologists).

It is important that LODOSYN with levodopa be taken at regular intervals according to the

schedule outlined by the health care provider. Caution patients not to change the prescribed

dosage regimen and not to add any additional antiparkinson medications, including other

carbidopa-levodopa preparations without first consulting a physician.

Advise patients that sometimes a ‘wearing-off’ effect may occur at the end of the dosing

Interval. Tell patients to notify the prescriber if such response poses a problem to lifestyle.

Patients should be advised that occasionally dark color (red, brown, or black) may appear in

saliva, urine, or sweat after ingestion of LODOSYN and levodopa. Although the color appears

to be clinically insignificant, garments may become discolored.

The patient should be advised that a change in diet to foods that are high in protein may delay

The absorption of levodopa and may reduce the amount taken up in the circulation. Excessive acidity also delays stomach emptying thus delaying the absorption of levodopa. Iron salts (such as in multivitamin tablets) may also reduce the amount of levodopa available in the body. The above factors may reduce the clinical effectiveness of the LODOSYN and levodopa therapy.

Alert patients to the possibility of sudden onset of sleep during daily activities, in some cases

without awareness or warning signs, when they are taking dopaminergic agents, including

levodopa. Advise patients to exercise caution while driving or operating machinery and that if

they have experience somnolence and/or sudden sleep onset, they must refrain from these

activities. (See WARNINGS, Falling Asleep During Activities of Daily Living and Somnolence

General.)

There have been reports of patients experiencing intense urges to gamble, increased sexual

urges, and other intense urges, and the inability to control these urges while taking one or more of the medications that increase central dopaminergic tone and that are generally used for the treatment of Parkinson’s disease, including LODOSYN and levodopa. Although it is not proven that the medications caused these events, these urges were reported to have stopped in some cases when the dose was reduced or the medication was stopped. Prescribers should ask patients about the development of new or increased gambling urges, sexual urges, or other intense urges while taking LODOSYN and levodopa. Physicians should consider dose reduction or stopping

Lodosyn and levodopa if a patient develops such urges while taking Lodosyn with carbidopa/levodopa (See PRECAUTIONS, Impulse Control/Compulsive Behaviors).

Laboratory Tests

Abnormalities in laboratory tests may include elevations of liver function tests such as alkaline phosphatase, SGOT (AST), SGPT (ALT), lactic dehydrogenase, and bilirubin. Abnormalities in blood urea nitrogen and positive Coombs test have also been reported. Commonly, levels of blood urea nitrogen, creatinine, and uric acid are lower during concomitant administration of carbidopa and levodopa than with levodopa alone.

Levodopa and carbidopa-levodopa combination products may cause a false-positive reaction for

urinary ketone bodies when a test tape is used for determination of ketonuria. This reaction will

not be altered by boiling the urine specimen. False-negative tests may result with the use of

glucose-oxidase methods of testing for glucosuria.

Drug Interactions

Caution should be exercised when the following drugs are administered concomitantly with LODOSYN (Carbidopa) given with levodopa or carbidopa-levodopa combination products.

Symptomatic postural hypotension has occurred when LODOSYN, given with levodopa or

carbidopa-levodopa combination products, was added to the treatment of a patient receiving antihypertensive drugs. Therefore, when therapy with LODOSYN, given with or without levodopa or carbidopa-levodopa combination products, is started, dosage adjustment of

the antihypertensive drug may be required.

For patients receiving monoamine oxidase inhibitors (Type A or B), see CONTRAINDICATIONS . Concomitant therapy with selegiline and carbidopa-levodopa may be associated with severe orthostatic hypotension not attributable to carbidopa-levodopa alone (see CONTRAINDICATIONS ).

There have been rare reports of adverse reactions, including hypertension and dyskinesia, resulting from the concomitant use of tricyclic antidepressants and carbidopa-levodopa preparations.

Dopamine D₂ receptor antagonists (e.g., phenothiazines, butyrophenones, risperidone) and isoniazid may reduce the therapeutic effects of levodopa. In addition, the beneficial effects of levodopa in Parkinson's disease have been reported to be reversed by phenytoin and papaverine. Patients taking these drugs with LODOSYN and levodopa or carbidopa-levodopa combination products should be carefully observed for loss of therapeutic response.

LODOSYN and iron salts or multi vitamins containing iron salts should be co administered

with caution. Iron salts can form chelates with levodopa and carbidopa and

consequently reduce the bioavailability of carbidopa and levodopa.

Although metoclopramide may increase the bioavailability of levodopa by increasing gastric emptying, metoclopramide may also adversely affect disease control by its dopamine receptor antagonistic properties.

Carcinogenesis, Mutagenesis, Impairment of Fertility

There were no significant differences between treated and control rats with respect to

mortality or neoplasia in a 96-week study of carbidopa at oral doses of 25, 45, or 135

mg/kg/day.Combinations of carbidopa and levodopa (10-20, 10-50, 10-100 mg/kg/day) were

given orally to rats for 106 weeks. No effect on mortality or incidence and type of neoplasia

was seen when compared to concurrent controls.

Mutagenicity studies have not been performed with either carbidopa or the combination of carbidopa and levodopa.

Carbidopa had no effect on the mating performance, fertility, or survival of the young when administered orally to rats at doses of 30, 60, or 120 mg/kg/day. The highest dose caused a moderate decrease in body weight gain in males.

The administration of carbidopa-levodopa at dose levels of 10-20, 10-50, or 10-100 mg/kg/day did not adversely affect the fertility of male or female rats, their reproductive performance, or the growth and survival of the young.

Pregnancy

Pregnancy Category C

There are no adequate and well-controlled studies with LODOSYN in pregnant women. It has been reported from individual cases that levodopa crosses the human placental barrier, enters the fetus, and is metabolized. Carbidopa concentrations in fetal tissue appeared to be minimal. LODOSYN should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Carbidopa, at doses as high as 120 mg/kg/day, was without teratogenic effects in the mouse or rabbit. In the rabbit, but not in the mouse, carbidopa-levodopa produced visceral anomalies, similar to those seen with levodopa alone, at approximately 7 times the maximum recommended human dose. The teratogenic effect of levodopa in rabbits was unchanged by the concomitant administration of carbidopa.

Nursing Mothers

It is not known whether carbidopa is excreted in human milk. Because many drugs are excreted in human milk, and because of their potential for serious adverse reactions in nursing infants, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the nursing woman.

Pediatric Use

Safety and effectiveness in pediatric patients have not been established, and use of the drug in patients below the age of 18 is not recommended.

Geriatric Use

Clinical studies of LODOSYN did not include sufficient numbers of subjects aged 65 and over

to determine whether they respond differently from younger subjects. Other clinical experience has not identified differences in responses between the elderly 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 concomitant disease and other drug therapy.

LODOSYN ADVERSE REACTIONS

Carbidopa has not been demonstrated to have any overt pharmacodynamic actions in the recommended doses. The only adverse reactions that have been observed have been with concomitant use of carbidopa with other drugs such as levodopa, and with carbidopalevodopa combination products.

When LODOSYN is administered concomitantly with levodopa or carbidopa-levodopa combination products, the most common adverse reactions have included dyskinesias such as choreiform, dystonic, and other involuntary movements, and nausea. Other adverse reactions reported with LODOSYN when administered concomitantly with levodopa alone or carbidopa-levodopa combination products were psychotic episodes including delusions, hallucinations, and paranoid ideation, depression with or without development of suicidal tendencies, and dementia. Convulsions also have occurred; however, a causal relationship with concomitant use of LODOSYN and levodopa has not been established.

The following other adverse reactions have been reported with levodopa and carbidopa-levodopa combination products. These same adverse reactions may also occur when LODOSYN is administered with these products.

Body as a Whole: abdominal pain and distress, asthenia, chest pain, fatigue.

Cardiovascular: cardiac irregularities, hypertension, myocardial infarction, hypotension including orthostatic hypotension, palpitation, phlebitis, syncope.

Gastrointestinal: anorexia, bruxism, burning sensation of the tongue, constipation, dark saliva, development of duodenal ulcer, diarrhea, dry mouth, dyspepsia, dysphagia, flatulence, gastrointestinal bleeding, gastrointestinal pain, heartburn, hiccups, sialorrhea, taste alterations, vomiting.

Hematologic: hemolytic and non-hemolytic anemia, leukopenia, thrombocytopenia, agranulocytosis.

Hypersensitivity: angioedema, urticaria, pruritus, Henoch-Schonlein purpura, bullous lesions (including pemphigus-like reactions).

Metabolic: edema, weight gain, weight loss.

Musculoskeletal: back pain, leg pain, muscle cramps, shoulder pain.

Nervous System/Psychiatric: Psychotic episodes including delusions, hallucinations and

paranoid ideation, neuroleptic malignant syndrome (NMS, see WARNINGS), bradykinetic

episodes (“on-off” phenomenon), confusion, agitation, dizziness, somnolence, dream

abnormalities including nightmares, insomnia, paresthesia, headache, depression with or without

development of suicidal tendencies, dementia, pathological gambling, increased libido including

hypersexuality, impulse control symptoms. Convulsions also have occurred; however, a causal

relationship with LODOSYN and levodopa, has not been established.

Skin: flushing, increased sweating, malignant melanoma (see also CONTRAINDICATIONS ), rash, alopecia, dark sweat.

Special Senses: oculogyric crises, diplopia, blurred vision, dilated pupils.

Urogenital: dark urine, priapism, urinary frequency, urinary incontinence, urinary retention, urinary tract infection.

Laboratory Tests: abnormalities in alkaline phosphatase, SGOT (AST), SGPT (ALT), lactic dehydrogenase, bilirubin, blood urea nitrogen (BUN), Coombs test; elevated serum glucose; decreased hemoglobin and hematocrit; decreased white blood cell count and serum potassium; increased serum creatinine and uric acid; white blood cells, bacteria and blood in the urine; protein and glucose in the urine.

Miscellaneous: bizarre breathing patterns, faintness, hoarseness, hot flashes, malaise, neuroleptic malignant syndrome, sense of stimulation.

OVERDOSAGE

No reports of overdose with LODOSYN have been received. Management of overdosage with carbidopa is the same as that with levodopa or carbidopa-levodopa preparations.

In the event of overdosage, general supportive measures should be employed, along with immediate gastric lavage. Intravenous fluids should be administered judiciously, and an adequate airway maintained. Electrocardiographic monitoring should be instituted and the patient carefully observed for the development of arrhythmias; if required, appropriate antiarrhythmic therapy should be given. The possibility that the patient may have taken other drugs as well as LODOSYN should be taken into consideration. To date, no experience has been reported with dialysis; hence, its value in overdosage is not known. Pyridoxine is not effective in reversing the actions of LODOSYN.

Based on studies in which high doses of levodopa and/or carbidopa were administered, a significant proportion of rats and mice given single oral doses of levodopa of approximately 1500-2000 mg/kg are expected to die. A significant proportion of infant rats of both sexes are expected to die at a dose of 800 mg/kg. A significant proportion of rats are expected to die after treatment with similar doses of carbidopa. The addition of carbidopa in a 1:10 ratio with levodopa increases the dose at which a significant proportion of mice are expected to die to 3360 mg/kg.

LODOSYN DOSAGE AND ADMINISTRATION

Whether given with carbidopa-levodopa or with levodopa, the optimal daily dose of

LODOSYN must be determined by careful titration. Most patients respond to a 1:10

proportion of carbidopa and levodopa, provided the daily dosage of carbidopa is 70 mg or

more a day. The maximum daily dosage of carbidopa should not exceed 200 mg, since

clinical experience with larger dosages is limited. If the patient is taking carbidopa-levodopa,

the amount of carbidopa in carbidopa-levodopa should be considered when calculating the

total amount of LODOSYN to be administered each day.

Patients Receiving Carbidopa-Levodopa Who Require Additional Carbidopa

Some patients taking carbidopa-levodopa may not have adequate reduction in nausea and

vomiting when the dosage of carbidopa is less than 70 mg a day, and the dosage of levodopa

is less than 700 mg a day. When these patients are taking carbidopa-levodopa, 25 mg of LODOSYN may be given with the first dose of carbidopa-levodopa each day. Additional doses of 12.5 mg or 25 mg may be given during the day with each dose of carbidopalevodopa. LODOSYN may be given with any dose carbidopa-levodopa as required for optimum therapeutic response. The maximum daily dosage of carbidopa, given as LODOSYN

and as carbidopa- levodopa), should not exceed 200 mg.

Patients Requiring Individual Titration of Carbidopa and Levodopa Dosage

Although carbidopa-levodopa is the most frequently used of carbidopa and levodopa

administration, there may be an occasional patient who requires individually titrated doses of

these two drugs. In these patients, LODOSYN (carbidopa) should be initiated at a dosage

of 25 mg three or four times a day. The two drugs should be given at the same time,

starting with no more than one-fifth (20%) to one-fourth (25%) of the previous or

recommended daily dosage of levodopa when given without LODOSYN (Carbidopa). In

patients already receiving levodopa therapy, at least twelve hours should elapse between

the last dose of levodopa and initiation of therapy with LODOSYN (Carbidopa) and

levodopa. A convenient way to initiate therapy in these patients is in the morning

following a night when the patient has not taken levodopa for at least twelve hours.

Health care providers who prescribe separate doses of LODOSYN and levodopa should be

thoroughly familiar with the directions for use of each drug.

Dosage Adjustment

Dosage of LODOSYN may be adjusted by adding or omitting one-half or one tablet a day. Because both therapeutic and adverse responses occur more rapidly with combined therapy than when only levodopa is given, patients should be monitored closely during the dose adjustment period. Specifically, involuntary movements will occur more rapidly when LODOSYN and levodopa are given concomitantly than when levodopa is given without LODOSYN. The occurrence of involuntary movements may require dosage reduction. Blepharospasm may be a useful early sign of excess dosage in some patients.

Current evidence indicates other standard antiparkinsonian drugs may be continued while carbidopa and levodopa are being administered. However, the dosage of such other standard antiparkinsonian drugs

may require adjustment.

Interruption of Therapy

Sporadic cases of hyperpyrexia and confusion have been associated with dose reductions and

withdrawal of carbidopa-Levodopa) or carbidopa-levodopa Extended Release. Patients should

be observed carefully if abrupt reduction or discontinuation of carbidopa-levodopa or

carbidopa-levodopa Extended-Release is required, especially if the patient is receiving

neuroleptics. (See WARNINGS .)

If general anesthesia is required, therapy may be continued as long as the patient is permitted to take fluids and medication by mouth. When therapy is interrupted temporarily, the patient should be observed for symptoms resembling NMS, and the usual daily dosage may be resumed as soon as the patient is able to take medication orally.

HOW SUPPLIED

Tablets LODOSYN, 25 mg, are orange, round, compressed tablets that are scored and coded

711 on one side and LODOSYN on the other.

They are supplied as follows:

NDC 25010-711-15 bottles of 100.

Storage

Store at 25°C (77°F), excursions permitted to 15–30°C (59–86°F).

Manufactured in Canada by:
Valeant Pharmaceuticals International, Inc.
Steinbach, MB R5G 1Z7
Canada

Manufactured for:
Aton Pharma, Inc. (division of Valeant Pharmaceuticals
North America LLC)
Bridgewater, NJ 08807 USA

Rev. 2/2014

LB0087-02

9379200

PRINCIPAL DISPLAY PANEL - 25 mg Tablet Bottle Label

Rx only

NDC 25010-711-15

LODOSYN ^®
(Carbidopa) Tablets

25 mg (Anhydrous equivalent)

100 Tablets

Valeant^®
Pharmaceuticals North America