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- Unit Price：
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Code：005380-002
- Tsumura Nijutsuto[88] : 42 sachets(for two weeks)
- $35.50
Up to 4 pieces per person
10% discount for total amount over $100
shipping schedule : about 3 weeks after payment
warehouse：Japan1
Manufacturer ：TSUMURA & CO.
Brand ：TSUMURA & CO.
JAN Code：----
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Description
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TSUMURA Nijutsuto Extract Granules (hereafter TJ-88)is in-dicated for the relief of the following symptoms:Frozen shoulder
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Presentation
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42 sachets
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Feature
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Granules
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Active Ingredients
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7.5 g(3sachets for 1day) of TSUMURA Nijutsuto extract granules con-tains 5.0 g of a dried extract of the following mixedcrude drugs.JP Pinellia Tuber 4.0gJP Atractylodes Lancea Rhizome 3.0gJP Clematis Root 2.5gJP Scutellaria Root 2.5gJP Cyperus Rhizome 2.5gJP Citrus Unshiu Peel 2.5gJP Atractylodes Rhizome 2.5gJP Poria Sclerotium 2.5gJP Glycyrrhiza 1.0gJP Ginger 1.0gArisaema Tuber 2.5gAralia Cordata Root 2.5g(JP: The Japanese Pharmacopoeia)
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Effect/Efficacy
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Frozen shoulder
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Usage/Dosage
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The usual adult dose is 7.5 g/day orally in 2 or 3 divided doses before or between meals. The dosage may be adjusted according to the patient's age and body weight, and symptoms.
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Cautions
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(1) When TJ-88 is used, the patient’s “SHO” (constitution/symptoms) should be taken into account. The patient’s progress should be carefully monitored, and if no improvement in symptoms/findings is observed, continuous treatment should be avoided. (2) Since TJ-88 contains Glycyrrhiza, careful attention should be paid to the serum potassium level, blood pressure, etc., and if any abnormality is observed, administration should be discontinued. (3) When TJ-88 is coadministered with other Kampo- preparations (Japanese traditional herbal medicines), etc., attention should be paid to the duplication of the contained crude drugs. SHO: The term “SHO” refers to a particular pathological status of a patient evaluated by the Kampo diagnosis, and is patterned according to the patient’s constitution, symptoms, etc. Kampo-preparations (Japanese traditional herbal medicines) should be used after confirmation that it is suitable for the identified “SHO” of the patient.
