Levodopa comp. B Stada indications
Treatment of Parkinson's disease.
Levodopa comp. B Stada dispersible is a formulation which is suitable for patients with dysphagia (difficulties in swallowing) or who require a formulation with a more rapid onset of action eg, patients suffering from early morning and afternoon akinesia, or who exhibit "delayed on" or "wearing off" phenomena.
Levodopa comp. B Stada HBS is indicated for patients presenting with all types of fluctuations (eg, "peak-dose dyskinesia" and "end of dose deterioration" eg, nocturnal immobility).
Levodopa comp. B Stada description
Levodopa comp. B Stada is a combination of Levodopa (Levodopa comp. B Stada) and the decarboxylase inhibitor besnerazide (as hydrochloride) in a ratio of 4:1 for the treatment of Parkinson's disease..
Levodopa comp. B Stada 62.5 is Levodopa (Levodopa comp. B Stada) 50 mg and Benserazide (Levodopa (Levodopa comp. B Stada) comp. B Stada) 12.5 mg; 125 is Levodopa (Levodopa comp. B Stada) 100 mg and Benserazide (Levodopa (Levodopa comp. B Stada) comp. B Stada) 25 mg; 250 is Levodopa (Levodopa comp. B Stada) 200 mg and besenrazide 50 mg.
Levodopa comp. B Stada 250: Each capsule contains Levodopa (Levodopa comp. B Stada) 200 mg and Benserazide (Levodopa (Levodopa comp. B Stada) comp. B Stada) HCl 50 mg.
Levodopa comp. B Stada HBS (Hydrodynamically Balanced System): Each capsule contains Levodopa (Levodopa comp. B Stada) 100 mg and Benserazide (Levodopa (Levodopa comp. B Stada) comp. B Stada) HCl 25 mg.
Levodopa comp. B Stada dosage
Standard
Dosage: Treatment with Levodopa comp. B Stada should be introduced gradually, dosage should be assessed individually and titrated for optimal effect. The following dosage instructions should therefore be regarded as guidelines.
Initial Therapy: In the early stages of Parkinson's disease it is advisable to start treatment with 1 capsule of Levodopa comp. B Stada '62.5' or half a tablet of Levodopa comp. B Stada '125' 3-4 times daily. As soon as tolerability of the initial dosing schedule is confirmed, the dosage should be increased slowly in accordance with the patient's response.
An optimal effect is generally achieved with a daily dosage of Levodopa comp. B Stada corresponding to Levodopa (Levodopa comp. B Stada) 300-800 mg + Benserazide (Levodopa (Levodopa comp. B Stada) comp. B Stada) 75-200 mg, to be divided into ≥3 doses. Between 4 and 6 weeks may be needed to achieve the optimal effect. If it proves necessary to further increase the daily dosage, this should be done on a monthly basis.
Maintenance Therapy: The average maintenance dosage is 1 capsule or tablet of Levodopa comp. B Stada '125' 3-6 times daily. The number of individual doses (not <3) and their distribution throughout the day must be titrated for optimal effect. Levodopa comp. B Stada HBS and Levodopa comp. B Stada dispersible may substitute standard Levodopa comp. B Stada to achieve an optimal effect.
Special Dosage Instructions: Dosage must be carefully titrated in all patients. Patients on other antiparkinsonian agents may receive Levodopa comp. B Stada. However, as treatment with Levodopa comp. B Stada proceeds and the therapeutic effect becomes apparent, the dosage of the other drugs may need to be reduced or these drugs gradually withdrawn.
Levodopa comp. B Stada dispersible tablets are particularly suitable for patients with dysphagia (difficulties in swallowing) or in situations where a more rapid onset of action is required eg, in patients suffering from early morning and afternoon akinesia or who exhibit "delayed on" or "wearing off" phenomena.
Patients who experience large fluctuations in the drug's effect in the course of the day (on-off phenomena) should receive smaller, more frequent single doses or be switched to Levodopa comp. B Stada HBS.
The switch from standard Levodopa comp. B Stada to Levodopa comp. B Stada HBS is preferably made from 1 day to the next, beginning with the morning dose. The daily dose and dosing interval should initially be the same as with standard Levodopa comp. B Stada.
After 2-3 days, the dosage should be gradually increased by about 50%. Patients should be informed that their condition may temporarily deteriorate.
Due to the pharmacokinetic properties of Levodopa comp. B Stada HBS, the onset of action is delayed. The clinical effect may be achieved more rapidly by administering Levodopa comp. B Stada HBS together with standard Levodopa comp. B Stada or Levodopa comp. B Stada dispersible. This may prove especially useful for the 1st morning dose, which should preferably be higher than the subsequent daily doses. The individual titration for Levodopa comp. B Stada HBS must be carried out slowly and carefully, allowing intervals of at least 2-3 days between dose changes.
In patients with nocturnal immobility, positive effects have been reported after gradually increasing the last evening dose to Levodopa comp. B Stada HBS 250 mg on retiring.
Excessive responses to Levodopa comp. B Stada HBS (dyskinesia) can be controlled by increasing the interval between doses rather than reducing the single doses.
Treatment with standard Levodopa comp. B Stada or Levodopa comp. B Stada dispersible should be resumed if the response to Levodopa comp. B Stada HBS is inadequate.
Patients should be carefully observed for possible undesirable psychiatric symptoms.
Administration: When taking standard Levodopa comp. B Stada capsules or Levodopa comp. B Stada HBS, patients must always ensure to swallow the whole capsule without chewing it.
Standard Levodopa comp. B Stada tablets are breakable to facilitate swallowing.
Levodopa comp. B Stada dispersible tablets are to be dispersed in a quarter of a glass of water (approximately 25-50 mL). The tablets disintegrate completely, producing a milky-white dispersion within a few minutes. Because of rapid sedimentation, it is advisable to stir the dispersion before drinking. Levodopa comp. B Stada dispersible tablets should be taken within ½ an hr of preparing the dispersion.
Levodopa comp. B Stada should be taken 30 min before or 1 hr after meals where possible. Undesirable gastrointestinal effects, which may occur mainly in the early stages of the treatment, can largely be controlled by taking Levodopa comp. B Stada with a small snack (eg, biscuits) or liquid or by increasing the dose slowly.
Levodopa comp. B Stada interactions
Pharmacokinetic Interactions: Co-administration of the anticholinergic drug trihexyphenidyl with standard Levodopa comp. B Stada reduces the rate, but not the extent of Levodopa (Levodopa comp. B Stada) absorption. Trihexyphenidyl given concomitantly with Levodopa comp. B Stada HBS does not affect the pharmacokinetics of Levodopa (Levodopa comp. B Stada).
Co-administration of antacids with Levodopa comp. B Stada HBS reduces the extent of Levodopa (Levodopa comp. B Stada) absorption by 32%.
Ferrous sulphate decreases the maximum plasma concentration and the AUC of Levodopa (Levodopa comp. B Stada) by 30-50%. The pharmacokinetic changes observed during co-treatment with ferrous sulphate appear to be clinically significant in some but not all patients.
Metoclopramide increases the rate of Levodopa (Levodopa comp. B Stada) absorption.
Domperidone may increase the bioavailability of Levodopa (Levodopa comp. B Stada) by stimulation of gastric emptying.
Pharmacodynamic Interactions: Neuroleptics, opioids and antihypertensive medications containing reserpine inhibit the action of Levodopa comp. B Stada.
If Levodopa comp. B Stada is to be administered to patients receiving irreversible nonselective MAO inhibitors, an interval of at least 2 weeks should be allowed between cessation of the MAO inhibitor and the start of Levodopa comp. B Stada therapy. Otherwise unwanted effects eg, hypertensive crises are likely to occur. Selective MAO-B inhibitors eg, selegiline and rasagiline and selective MAO-A inhibitors eg, moclobemide, can be prescribed to patients on Levodopa comp. B Stada therapy; it is recommended to readjust the Levodopa (Levodopa comp. B Stada) dose to the individual patient's needs, in terms of both efficacy and tolerability. Combination of MAO-A and MAO-B inhibitors is equivalent to nonselective MAO inhibition and hence this combination should not be given concomitantly with Levodopa comp. B Stada.
Levodopa comp. B Stada should not be administered concomitantly with sympathomimetics (agents eg, epinephrine, norepinephrine, isoproterenol or amphetamine which stimulate the sympathetic nervous system) as Levodopa (Levodopa comp. B Stada) may potentiate their effects. Should concomitant administration prove necessary, close surveillance of the cardiovascular system is essential, and the dose of the sympathomimetic agents may need to be reduced.
Combination with other agents eg, anticholinergics, amantadine, selegiline,bromocriptine and dopamine agonists is permissible, though both the desired and the undesired effects of treatment may be intensified. It may be necessary to reduce the dosage of Levodopa comp. B Stada or the other substance. When initiating an adjuvant treatment with a COMT inhibitor, a reduction of the dosage of Levodopa comp. B Stada may be necessary. Anticholinergics should not be withdrawn abruptly when Levodopa comp. B Stada therapy is instituted, as Levodopa (Levodopa comp. B Stada) does not begin to take effect for some time.
Levodopa (Levodopa comp. B Stada) may affect the results of laboratory tests for catecholamines, creatinine, uric acid and glucose.
Coombs' tests may give a false-positive result in patients taking Levodopa comp. B Stada.
Concomitant administration of antipsychotics with dopamine-receptor blocking properties, particularly D2-receptor antagonists might antagonize the antiparkinsonian effects of Levodopa (Levodopa comp. B Stada)-Benserazide (Levodopa (Levodopa comp. B Stada) comp. B Stada). Levodopa (Levodopa comp. B Stada) may reduce antipsychotic effects of these drugs. These drugs should be co-administration with caution.
A diminution of effect is observed when the drug is taken with a protein-rich meal.
General Anesthesia with Halothane: Levodopa comp. B Stada should be discontinued 12-48 hrs before surgical intervention requiring general anesthesia with halothane as fluctuations in blood pressure and/or arrhythmias may occur.
For general anesthesia with other anesthetics see Precautions.
Levodopa comp. B Stada side effects
Post-Marketing: Blood and Lymphatic System Disorders: Hemolytic anemia, transient leukopenia and thrombocytopenia have been reported in rare cases. Therefore, as in any long-term Levodopa (Levodopa comp. B Stada)-containing treatment, blood count and liver and kidney function should be monitored periodically.
Metabolic and Nutritional Disorders: Anorexia has been reported.
Psychiatric Disorders: Depression can be part of the clinical picture in patients with Parkinson's disease and may also occur in patients treated with Levodopa comp. B Stada. Agitation, anxiety, insomnia, hallucinations, delusions and temporal disorientation may occur particularly in elderly patients and in patients with a history of such disorders.
Nervous System Disorder: Isolated cases of ageusia or dysgeusia have been reported. At later stages of the treatment, dyskinesia (eg, choreiform or athetotic) may occur. These can usually be eliminated or be made tolerable by a reduction of dosage. With prolonged treatment, fluctuations in therapeutic response may also be encountered.
They include freezing episodes, end-of-dose deterioration and the "on-off" effect. These can usually be eliminated or made tolerable by adjusting the dosage and by giving smaller single doses more frequently. An attempt at increasing the dosage again can subsequently be made in order to intensify the therapeutic effect. Levodopa comp. B Stada is associated with somnolence and has been associated very rarely with excessive daytime somnolence and sudden sleep onset episodes.
Cardiac Disorders: Cardiac arrhythmias may occur occasionally.
Vascular Disorders: Orthostatic hypotension may occur occasionally. Orthostatic disorders commonly improve following reduction of the Levodopa comp. B Stada dosage.
Gastrointestinal Disorders: Nausea, vomiting and diarrhea have been reported with Levodopa comp. B Stada. Undesirable gastrointestinal effects, which may occur mainly in the early stages of the treatment, can largely be controlled by taking Levodopa comp. B Stada with some food or liquid or by increasing the dose slowly.
Skin and Subcutaneous Tissue Disorders: Allergic skin reactions eg, pruritus and rash may occur in rare cases.
Investigations: Transient elevation of liver transaminase and alkaline phosphatase may occur. Increase of γ-glutamyltransferase has been reported.
Rises in blood urea nitrogen have been noted with Levodopa comp. B Stada.
Urine may be altered in color, usually acquiring a red tinge which turns dark on standing. Other body fluids or tissues may also be discoloured or stained including saliva, the tongue, teeth or oral mucosa.
Laboratory Abnoramlities: See Post-Marketing as previously mentioned.
Levodopa comp. B Stada contraindications
Hypersensitivity to Levodopa (Levodopa comp. B Stada) or Benserazide (Levodopa (Levodopa comp. B Stada) comp. B Stada).
In conjunction with nonselective monoamine oxidase (MAO) inhibitors. However, selective MAO-B inhibitors eg, selegiline and rasagiline or selective MAO-A inhibitors eg, moclobemide are not contraindicated. Combination of MAO-A and MAO-B inhibitors is equivalent to nonselective MAO inhibition and hence, this combination should not be given concomitantly with Levodopa comp. B Stada.
Patients with decompensated endocrine, renal (except patients on dialysis) or hepatic function, cardiac disorders, psychiatric diseases with a psychotic component or closed angle glaucoma.
Pregnant women or to women of childbearing potential in the absence of adequate contraception. If pregnancy occurs in a woman taking Levodopa comp. B Stada, the drug must be discontinued (as advised by the prescribing physician).
Patients <25 years (skeletal development must be complete).
Use in pregnancy: Levodopa comp. B Stada is contraindicated during pregnancy and in women of childbearing potential in the absence of adequate contraception.
Active ingredient matches for Levodopa comp. B Stada:
Benserazide/Levodopa in Germany.
List of Levodopa comp. B Stada substitutes (brand and generic names) | Sort by popularity |
| Unit description / dosage (Manufacturer) | Price, USD |
| Levodopa/Benserazide PCH (Netherlands) | |
| Levopar (Germany, Indonesia, Israel) | |
| Capsule; Oral; Benserazide 12.5 mg; Levodopa 50 mg (M & H Manufacturing) | |
| Capsule; Oral; Benserazide 25 mg; Levodopa 100 mg (M & H Manufacturing) | |
| Capsule; Oral; Benserazide 50 mg; Levodopa 200 mg (M & H Manufacturing) | |
| Levopar 5 x 10's (M & H Manufacturing) | $ 24.80 |
| Levopar tab 250 mg 10 x 10's (M & H Manufacturing) | |
| Levopar Plus (Israel) | |
| Capsule; Oral; Benserazide Hydrochloride 25 mg; Levodopa 100 mg (Teva) | |
| Levopar Plus 125 (Israel) | |
| Levopar Plus 250 (Israel) | |
| LEVOSTAL (Peru) | |
| LEVOSTAL 250MG TABLET 1 strip / 10 tablets each (Stallion Laboratories Pvt Ltd) | $ 0.45 |
| LEVOSTAL 500MG TABLET 1 strip / 10 tablets each (Stallion Laboratories Pvt Ltd) | $ 0.91 |
| Levostal 500mg Tablet (Stallion Laboratories Pvt Ltd) | $ 0.09 |
| Levostal 750mg Tablet (Stallion Laboratories Pvt Ltd) | $ 0.14 |
| Madopar (Albania, Argentina, Armenia, Aruba, Australia, Austria, Azerbaijan, Bahrain, Belarus, Bolivia, Bosnia & Herzegowina, Brazil, Bulgaria, Cambodia, Chile, China, Colombia, Cote D'ivoire, Croatia (Hrvatska), Cuba, Czech Republic, Denmark, Dominican Republic, Estonia, Ethiopia, Finland, Georgia, Germany, Greece, Guinea, Hong Kong, Hungary, Iceland, Indonesia, Iran, Ireland, Italy, Jamaica, Japan, Kazakhstan, Laos, Latvia, Lebanon, Libya, Lithuania, Luxembourg, Malaysia, Malta, Mauritania, Mauritius, Mexico, Moldova, Morocco, Netherlands, New Zealand, Norway, Oman, Paraguay, Peru, Philippines, Poland, Portugal, Romania, Russian Federation, Saudi Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sri Lanka, Switzerland, Syria, Taiwan, Thailand, Trinidad & Tobago, Turkey, Turkmenistan, United Kingdom, Uruguay, Uzbekistan, Venezuela, Vietnam) | |
| Capsule; Oral; Levodopa 50 mg; Benserazide Hydrochloride 12.5 mg (Abbott) | |
| Capsule; Oral; Levodopa 100 mg; Benserazide Hydrochloride 25 mg (Abbott) | |
| Capsule; Oral; Levodopa 200 mg; Benserazide Hydrochloride 50 mg (Abbott) | |
| Tablet, Dispersible; Oral; Levodopa 100 mg; Benserazide Hydrochloride 25 mg (Abbott) | |
| Tablet; Oral; Levodopa 100 mg; Benserazide Hydrochloride 25 mg (Abbott) | |
| Tablet; Oral; Levodopa 200 mg; Benserazide Hydrochloride 50 mg (Abbott) | |
| Madopar Dispersible 100's (Abbott) | |
| Madopar HBS 100's (Abbott) | |
| Madopar 100's (Abbott) | |
| Madopar 125 125 mg x 100's (Abbott) | |
| Madopar 125 125 mg x 1000's (Abbott) | |
| Madopar 250 250 mg x 100's (Abbott) | |
| Madopar 250 250 mg x 1000's (Abbott) | |
| Madopar HBS 125 mg x 100's (Abbott) | $ 51.87 |
| Madopar HBS 125 mg x 1000's (Abbott) | |
| Madopar 250 100's (Abbott) | $ 68.11 |
| Madopar Dispersible 125 100's (Abbott) | |
| Madopar 125 1000's (Abbott) | |
| Madopar 250 100 Tablet (Abbott) | |
| Madopar HBS 100 Tablet (Abbott) | |
| Madopar 125 125 mg x 1's (Abbott) | |
| Madopar 250 250 mg x 1's (Abbott) | |
| Madopar Dispersible 125 125 mg x 100's (Abbott) | |
| Madopar 62.5 mg x 30 Tablet (Abbott) | |
| Madopar 62.5 mg x 100 Tablet (Abbott) | |
| Madopar 125 mg x 30 Tablet (Abbott) | |
| Madopar 125 mg x 100 Tablet (Abbott) | |
| Madopar 250 mg x 30 Tablet (Abbott) | |
| Madopar 250 mg x 100 Tablet (Abbott) | |
| Madopar 30 Tablet (Abbott) | |
| Madopar 100 Tablet (Abbott) | |
| MADOPAR TABLET 1 strip / 10 tablets each (Abbott) | $ 1.78 |
| MADOPAR tab 10's (Abbott) | $ 1.29 |
| Madopar HBS cap 100's (Abbott) | |
| Madopar 250 tab 100's (Abbott) | |
| Madopar Tablet (Abbott) | $ 0.21 |
| Madopar 100 mg/25 mg (Hungary) | |
| Madopar 100 mg/25 mg retard (Hungary) | |
| Madopar 125 (Australia, Denmark) | |
See 175 substitutes for Levodopa comp. B Stada | |
References
- DailyMed. "CARBIDOPA; ENTACAPONE; LEVODOPA: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
- PubChem. "levodopa". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
- PubChem. "benserazide". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
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