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Progressive Myoclonus Epilepsy

Treatment No. : RD0701
Dosage & Instructions: Two tablets twice a day.
Composition:
Corallium rubraum D3
Atropinum sulfur D4
Cuprum aceticum D4
Magnesia phosph D3
Arsenicum album D4
Zincum valeriana D4
Agnus castus D3
Silicea D5
Treatment Type:
This remedy is a symptomatic treatment. A symptomatic treatment cannot eliminate the disease from its root but is able to considerably improve the patient's condition by easing his or her symptoms.
Contra-indications: None established
Special Instructions: Whereas this remedy can be safely used by teenagers, its use has not been evaluated in children under 12 years of age. Please do not administer to children under this age.
Storage: Store in a cool and dry place
Precautions: Keep away from the reach of children
Standard Packaging : 60 Tabs

Order Online:

One 60 tabs bottle for $79.99
Two 60 tabs bottles for $129.99

 

Condition Overview:

Progressive Myoclonus Epilepsy (PME) is a syndrome involving the central nervous system and representing more than a dozen different diseases. These diseases share certain features, including a worsening of symptoms over time and the presence of both muscle contractions (myoclonus) and seizures (epilepsy). Patients may have more than one type of seizure, such as petit mal or grand mal. PME is progressive, but the rate of progression may be quick or slow, depending on the underlying disease.

Progressive Myoclonus Epilepsy (PME) is different from myoclonic epilepsy. In myoclonic epilepsy, the myoclonic jerking motions occur as part of the seizure. In PME, myoclonus occurs separately from seizures, the two respond differently to the same drugs, they evolve differently during the natural history of the disease, and they cause different problems for the patient. Some drugs that are good for seizures, e.g. phenytoin and carbamazepine, may tend to make the myoclonus worse.
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