GNH USA

Europe — EMA

Neodolpasse (Diclofenac Sodium, Orphenadrine Citrate)

GNH USA supplies Neodolpasse (Diclofenac sodium and orphenadrine citrate), a non‑steroidal anti‑inflammatory and muscle relaxant for moderate to severe pain

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What is Diclofenac Sodium, Orphenadrine Citrate?

Diclofenac sodium and orphenadrine citrate, the active ingredient in Neodolpasse, is a non‑steroidal anti‑inflammatory drug and muscle relaxant presented as a sterile injectable solution for intravenous use. It is used to manage moderate to severe pain, inflammatory conditions, and muscle spasm in adult patients.

GNH USA supplies Neodolpasse as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Diclofenac Sodium, Orphenadrine Citrate used for?

Neodolpasse combines an NSAID and a muscle relaxant to address pain‑related pathways and spastic muscle conditions.

- Moderate to severe pain: provides analgesia by reducing inflammation and relaxing skeletal muscle. - Inflammatory conditions: diminishes prostaglandin‑mediated swelling and discomfort. - Muscle spasm: alleviates involuntary muscle contractions through anticholinergic and NMDA‑receptor antagonism.

What are the side effects of Diclofenac Sodium, Orphenadrine Citrate?

Adverse reactions may occur with any intravenous NSAID‑muscle‑relaxant combination.

Common Side Effects: - Injection site pain or erythema - Nausea or dyspepsia - Dizziness or headache - Mild transient hypotension - Elevated liver enzymes - Dry mouth or blurred vision

Serious or Rare Side Effects: - Severe gastrointestinal bleeding or ulceration - Anaphylactic or severe hypersensitivity reactions - Hepatotoxicity with marked transaminase rise - Renal impairment or acute kidney injury - Cardiac arrhythmias or myocardial infarction - Severe thrombocytopenia or coagulation disorders

What precautions apply to Diclofenac Sodium, Orphenadrine Citrate?

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor for adverse events.

- Assess renal and hepatic function: adjust use in impairment. - Review cardiovascular history: NSAIDs may increase thrombotic risk. - Evaluate for gastrointestinal ulcer disease: consider gastro‑protective measures. - Screen for asthma or allergic reactions to NSAIDs. - Monitor for signs of bleeding or hematologic abnormalities. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

What does Diclofenac Sodium, Orphenadrine Citrate interact with?

Neodolpasse may interact with several drug classes, requiring careful management.

Major Interactions (Avoid): - Anticoagulants (e.g., warfarin): increased bleeding risk. - Other NSAIDs or COX‑2 inhibitors: additive gastrointestinal toxicity. - Lithium: diclofenac may raise serum lithium levels. - Methotrexate: reduced clearance leading to toxicity. - ACE inhibitors or ARBs: heightened risk of renal impairment.

Moderate Interactions (Monitor Closely): - Diuretics: possible reduction in renal perfusion. - SSRIs or SNRIs: modest increase in bleeding tendency. - Corticosteroids: synergistic ulcerogenic effect. - Beta‑blockers: potential for additive hypotensive effect. - Anticholinergic drugs: may enhance dry‑mouth or blurred‑vision symptoms.

Frequently asked questions

What conditions is Neodolpasse used to treat?+
Neodolpasse is indicated for the management of moderate to severe pain, inflammatory conditions such as arthritis or postoperative inflammation, and skeletal muscle spasm. It combines an NSAID with a muscle relaxant to address both pain and involuntary muscle contractions.
How does diclofenac sodium and orphenadrine citrate work together?+
Diclofenac sodium inhibits COX‑1 and COX‑2 enzymes, reducing prostaglandin production and thereby decreasing inflammation and pain. Orphenadrine citrate acts as an anticholinergic and NMDA‑receptor antagonist, providing skeletal muscle relaxation. The dual mechanism offers analgesia and spasm relief.
What is the usual dose of Neodolpasse?+
The specific dose and infusion rate of Neodolpasse are determined by the prescribing clinician based on the patient’s condition, weight, renal and hepatic function, and response to therapy. Dosage should follow the prescriber’s instructions and local guidelines.
Is Neodolpasse safe to use during pregnancy or breastfeeding?+
Safety data for Neodolpasse in pregnancy and lactation are limited. Diclofenac may affect fetal renal function, and orphenadrine can cross the placenta. Use only if the potential benefit justifies the potential risk, and consult a healthcare professional before administration.
How do I order Neodolpasse from GNH USA?+
To order Neodolpasse, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where applicable), and import documentation.
How does Neodolpasse compare with other NSAID‑muscle‑relaxant combinations?+
Neodolpasse uniquely combines diclofenac, a potent COX inhibitor, with orphenadrine, an anticholinergic muscle relaxant. Compared with other combinations, it offers both strong anti‑inflammatory action and targeted muscle relaxation in a single intravenous formulation, potentially reducing the need for multiple agents.
What are the recommended storage conditions for Neodolpasse?+
Neodolpasse should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the product in its original packaging to maintain sterility and potency.
How is Neodolpasse administered?+
Neodolpasse is administered intravenously by a qualified healthcare professional. The solution is typically infused over a prescribed period, with the rate and total volume determined by the prescriber’s orders and patient monitoring.
What are the most serious risks associated with Neodolpasse?+
Serious risks include severe gastrointestinal bleeding or ulceration, anaphylactic reactions, hepatotoxicity, renal impairment, and cardiovascular events such as myocardial infarction. Patients should be monitored closely for signs of these adverse events.
Who should not receive Neodolpasse?+
Neodolpasse is contraindicated in patients with known hypersensitivity to diclofenac, orphenadrine, or any component of the formulation, as well as those with active gastrointestinal bleeding, severe renal or hepatic impairment, and certain cardiovascular conditions. Clinicians should assess each patient’s medical history before prescribing.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Diclofenac Sodium, Orphenadrine Citrate
Route
Intravenous Use
Manufacturer
Fresenius Kabi S.R.O.
Origin
EU

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