Overview of Viadil Compuesto
| Property | Description |
|---|---|
| Active Ingredients | Pargeverine hydrochloride, Sodium Metamizole |
| Form | Tablet, Injectable Solution, Oral Solution (Drops) |
| Pharmacological Class | Antispasmodic Agent & Non-Opioid Analgesic |
| Common Use | Relief of pain associated with muscle spasms |
| Origin | Synthetic |
Defining Viadil Compuesto: Identity, Type, and Class
Viadil Compuesto is a synthetic fixed-dose combination product formally classified as an antispasmodic agent and a potent non-opioid analgesic with established antipyretic properties. This dual classification defines its fundamental therapeutic identity, establishing it as a medicine specifically designed to address pain and visceral muscle spasm concurrently. The combination of its active components, Pargeverine hydrochloride and Sodium Metamizole, allows it to target two distinct physiological actions simultaneously, distinguishing it from single-entity drugs. Its components are purely synthetic in origin, chemically manufactured to pharmaceutical standards. Viadil Compuesto is often prescribed across Latin American territories as a standard treatment for acute abdominal or urinary tract cramping.
Composition and General Therapeutic Purpose
The product is composed of two principal active ingredients: Pargeverine hydrochloride, which acts as the primary spasmolytic agent, and Sodium Metamizole (also recognized as Dipyrone), which is a pyrazolone derivative contributing powerful analgesic and antipyretic effects. Sodium Metamizole is a non-acid, non-opioid pain reliever effective for relieving pain and reducing fever.
The overarching purpose of Viadil Compuesto is the rapid and reliable relief of severe, acute pain that is intrinsically linked to painful visceral muscle spasms or cramps. This combination approach is used for providing relief in conditions such as renal or biliary colic. Its core benefit derives from the combination of a dedicated spasmolytic agent and a strong non-opioid analgesic, allowing the medicine to simultaneously relax the constricted internal muscle and block the transmission of the resulting pain signal. This dual-action mechanism is intended for acute spasm-related discomfort, with the analgesic component providing utility for acute pain situations.
Regulatory References

