PSORIZIDE ULTRA- potassium bromide, nickel sulfate, and zinc bromide tablet

国: アメリカ合衆国

言語: 英語

ソース: NLM (National Library of Medicine)

有効成分:

POTASSIUM BROMIDE (UNII: OSD78555ZM) (BROMIDE ION - UNII:952902IX06), NICKEL SULFATE (UNII: 4FLT4T3WUN) (NICKEL CATION - UNII:OIS2CXW7AM), ZINC BROMIDE (UNII: OO7ZBU9703) (ZINC CATION - UNII:13S1S8SF37)

から入手可能:

PLYMOUTH HEALTHCARE PRODUCTS LLC

INN（国際名）:

Potassium Bromide

構図:

Potassium Bromide 1 [hp_X]

投与経路:

ORAL

処方タイプ:

PRESCRIPTION DRUG

適応症:

PSORIZIDE ® ULTRA is indicated for the treatment of moderate to severe eczema, atopic dermatitis, seborrhea and seborrheic dermatitis. It has been found to work well with variety of combination therapies. Psoriasis also responds, but generally has a more favorable response to PSORIZIDE ® Forte (NDC 61480-255-05.) Although there are no known contraindications, patients who are allergic to any PSORIZIDE ® ULTRA ingredient should consult a physician prior to taking the medication. (Refer to Section on Hypersensitivity)

製品概要:

Scored tablets, off white in color with green speckles, with LL and score imprinted on same side, in child-resistant and tamper-resistant bottles of 100. NDC 61480-124-05.

認証ステータス:

unapproved homeopathic

製品の特徴

PSORIZIDE ULTRA- POTASSIUM BROMIDE, NICKEL SULFATE, AND ZINC
BROMIDE TABLET
PLYMOUTH HEALTHCARE PRODUCTS LLC
_Disclaimer: This homeopathic product has not been evaluated by the
Food and Drug_
_Administration for safety or efficacy. FDA is not aware of scientific
evidence to support_
_homeopathy as effective._
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PSORIZIDE ULTRA
CAUTION: Federal law prohibits dispensing without a prescription.
DESCRIPTION
PSORIZIDE
ULTRA is a biochemical homeopathic medication indicated for the
TREATMENT OF ECZEMA AND SEBORRHEA.
The active ingredients in each
PSORIZIDE
ULTRA tablet consist of the following: Potassium Bromide (Kali
Bromatum)
1X, Nickel Sulphate (Niccolum Sulphuricum) 1X and Zinc Bromide (Zincum
Bromatum)
4x. These drug ingredients are listed in the Homoeopathic
Pharmacopoeia of the United
States (HPUS).
Inactive ingredients: Lactose and Magnesium Stearate.
PHARMACOLOGICAL CLASS: Homeopathic drug
DOSAGE FORM: Oral 300 mg scored tablet. May be swallowed whole, chewed
or
dissolved in the mouth and swallowed.
CLINICAL PHARMACOLOGY
The active ingredients in PSORIZIDE
ULTRA are inorganic soluble mineral salts. The
exact mechanism of action is unknown; however, it is believed
PSORIZIDE
ULTRA
addresses a primary genetic biochemical defect.
POTASSIUM BROMIDE dissolves and dissociates in the digestive tract
into its ionic
constituents. Each tablet contains approximately 15 mg bromide
(calculated). Ionic
bromide is rapidly and completely absorbed from the intestine and
distributed almost
exclusively in the extracellular fluids.
Bromide is eliminated by the kidneys and the
elimination half-life is 11-12 days. "Once a day" dosing will lead to
a steady state
concentration in about seven weeks.
NICKEL SULPHATE dissolves and dissociates in the digestive tract into
its ionic
constituents. Each tablet contains approximately 1.5 mg of ionic
nickel (calculated).
According to studies, 15% to 50% of ionic nickel is absorbed on a
fasted stomach.
Food markedly decreases the rate and extent of nickel absorption.
Clinical studies
sh