Zeel
Zeel 2.0 ml Injection
FULL PRESCRIBING INFORMATION: CONTENTS*
- ZEEL DESCRIPTION
- ZEEL INDICATIONS AND USAGE
- ZEEL DOSAGE AND ADMINISTRATION
- ZEEL CONTRAINDICATIONS
- WARNINGS AND PRECAUTIONS
- ZEEL ADVERSE REACTIONS
- OVERDOSAGE
- CLINICAL PHARMACOLOGY
- DOSAGE
FULL PRESCRIBING INFORMATION
ZEEL DESCRIPTION
Each 2.0 ml ampule contains: | |||
Active Ingredients: | |||
Ingredient name | Potency | Quantity | Final dilution |
a-Lipoicum acidum | 8X | 2.0 μl | 10.99X |
Arnica montana, radix | 4X | 200.0 μl | 5.00X |
Cartilago suis | 6X | 2.0 μl | 9.00X |
Coenzyme A | 8X | 2.0 μl | 10.99X |
Dulcamara | 3X | 10.0 μl | 5.30X |
Embryo totalis suis | 6X | 2.0 μl | 9.00X |
Funiculus umbilicalis suis | 6X | 2.0 μl | 9.00X |
Nadidum | 8X | 2.0 μl | 10.99X |
Natrum oxalaceticum | 8X | 2.0 μl | 10.99X |
Placenta suis | 6X | 2.0 μl | 9.00X |
Rhus toxicodendron | 2X | 10.0 μl | 4.30X |
Sanguinaria canadensis | 4X | 3.0 μl | 6.82X |
Sulphur | 6X | 3.6 μl | 8.74X |
Symphytum officinale | 6X | 10.0 μl | 8.30X |
Inactive Ingredients
Water for injection 1,747.4 μl
Sodium Chloride 17.6 μl
ZEEL INDICATIONS AND USAGE
Treatment of arthrosis/osteoarthritis, and/or rheumatic joint diseases
- Zeel® Injection Solution is a homeopathic drug product indicated for the treatment of arthrosis/osteoarthritis, and/or rheumatic joint diseases and for the relief of symptoms such as pain and joint stiffness.
Co-administration Therapy with Traumeel® Injection Solution for the treatment of inflammatory and degenerative conditions of the musculoskeletal system.
- Zeel® Injection Solution is a homeopathic drug product indicated, in combination with Traumeel® Injection Solution, for the treatment of inflammatory and degenerative conditions of the musculoskeletal system, such as arthrosis/osteoarthritis and/or rheumatic joint diseases, and for the relief of symptoms including pain, swelling, and joint stiffness.
ZEEL DOSAGE AND ADMINISTRATION
General Considerations
- The dosage schedules listed below can be used as a general guide for the administration of Zeel® Injection Solution.
- Zeel® Injection Solution may be administered s.c., i.d., i.m., i.a. or i.v.
- The interval between injections is left to the discretion of the HCP, but should not exceed 1 ampule in 24 hours.
- Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Draw up the contents of the ampule into the syringe. Discard half or one third of the contents, depending on the required dosage, before administering.
Standard Dosage - for the treatment of arthrosis/osteoarthritis and/or rheumatic joint diseases and for the relief of symptoms such as pain and joint stiffness.
Adults and children 12 years and older:
1 ampule 1 to 3 times per 7 days
Children 6 to 11 years:
2/3 of an ampule 1 to 3 times per 7 days
Acute Dosage - for the treatment of arthrosis/osteoarthritis and/or rheumatic joint diseases and for the relief of symptoms such as pain and joint stiffness.
Adults and children 12 years and older:
1 ampule daily, and then continue with standard dosage
Children 6 to 11 years:
2/3 of an ampule daily, and then continue with standard dosage
Co-administration therapy with Traumeel® Injection Solution - for the treatment of inflammatory and degenerative conditions of the musculoskeletal system, such as arthrosis/osteoarthritis and/or rheumatic joint diseases, and for the relief of symptoms including pain, swelling, and joint stiffness.
- In the treatment of musculoskeletal conditions, if co-administration with another homeopathic medicinal product is desired, Zeel® Injection Solution may be mixed in a ratio of 1:1 with Traumeel® Injection Solution.
- For convenience, the daily dose of Zeel® Injection Solution may be administered at the same time as a Traumeel® Injection Solution, according to the dosing recommendations for each medication.
ZEEL CONTRAINDICATIONS
- Zeel® Injection Solution is contraindicated in patients with known hypersensitivity to Zeel® or any of its ingredients.
- When Zeel® Injection Solution is co-administered with Traumeel® Injection Solution, refer to the Contraindication section of the respective Traumeel® Injection Solution labeling.
WARNINGS AND PRECAUTIONS
Keep out of reach of children.
ZEEL ADVERSE REACTIONS
Post Marketing Experience
- The following adverse events have been identified during post-marketing use of Zeel® Injection Solution. Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frquency or establish a causal relationship to drug exposure.
- Adverse event rates observed in Monotherapy use of Zeel® Injection Solution: Allergic (hypersensitivity) skin reactions may occur in isolated cases.
- Adverse event rates observed in the Monotherapy use of Traumeel® Injection Solution: Allergic (hypersensitivity) reactions (e.g. skin allergies, redness/swelling at the injection site, even up to anaphylaxis) may occur in isolated cases.
To report SUSPECTED ADVERSE REACTIONS, contact Heel Inc. at 1.800.920.9203
info@heelusa.com or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
OVERDOSAGE
No negative effects of an overdose have been reported and none are expected due to the homeopathic dilutions.
CLINICAL PHARMACOLOGY
Mechanism of Action
The exact mechanism of Zeel® Injection Solution is not fully understood.
Pharmacodynamics
Not applicable for homeopathic medicinal products.
DOSAGE
One ampule containing 2.0 ml each containing the active ingredients in the strengths listed under Description.
ZeelARNICA MONTANA ROOT, TOXICODENDRON PUBESCENS LEAF, SOLANUM DULCAMARA TOP, COMFREY ROOT, SULFUR, SANGUINARIA CANADENSIS ROOT, SUS SCROFA CARTILAGE, SUS SCROFA EMBRYO, SUS SCROFA UMBILICAL CORD, SUS SCROFA PLACENTA, .ALPHA.-LIPOIC ACID, COENZYME A, NADIDE and SODIUM DIETHYL OXALACETATE INJECTION
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