Meftal Spas
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Last updated: June 2025
For educational purposes only
Clinical Reference
# Meftal spas
## Overview
- **Classification**: Combination product containing a **Non-Steroidal Anti-Inflammatory Drug (NSAID)** (Mefenamic Acid) and an **Anticholinergic/Antispasmodic** (Dicyclomine HCl).
- **Mechanism**: Mefenamic Acid inhibits cyclooxygenase (COX-1 & COX-2), reducing prostaglandin synthesis for pain and inflammation. Dicyclomine HCl is an anticholinergic that blocks muscarinic receptors and has direct smooth muscle relaxant effects, reducing muscle spasms.
## Primary Indications
1. **Dysmenorrhea**: Relief of spasmodic pain associated with menstruation.
2. **Intestinal Colic/Spasms**: Management of spasmodic pain in the gastrointestinal tract.
3. **Biliary/Renal Colic**: Adjunctive relief of pain due to smooth muscle spasms.
## Adult Dosing
### Standard Dosing
**Dysmenorrhea / Intestinal Colic**
- **Dose**: **1 tablet** (typically containing Mefenamic Acid **250 mg** + Dicyclomine HCl **10 mg**)
- **Frequency**: Up to **3 times daily**
- **Route**: Oral
- **Duration**: Short-term use, typically **3-5 days** for acute pain.
### Dose Adjustments
- **Renal Impairment**: **Caution**; reduce dose or avoid in moderate to severe impairment (CrCl <30 mL/min) due to Mefenamic Acid. Dicyclomine excretion also affected.
- **Hepatic Impairment**: **Caution/Contraindicated** in severe impairment; monitor liver function. Both components are metabolized by the liver.
- **Elderly Patients**: Use with **extreme caution**; lower doses may be required due to increased sensitivity to adverse effects (especially anticholinergic effects and renal/GI risks). Avoid if possible.
## Pediatric Dosing
### Neonates (0-28 days)
- **Dose**: **Contraindicated**.
- **Special Notes**: Dicyclomine is absolutely contraindicated in infants <6 months due to severe risk of respiratory depression, apnea, seizures, and SIDS. Mefenamic acid is also generally not recommended.
### Infants (1-12 months)
- **Dose**: **Contraindicated**.
- **Special Notes**: Dicyclomine is absolutely contraindicated in infants <6 months. High risk of severe anticholinergic effects.
### Children (1-12 years)
- **Dose**: **Generally not recommended** for routine use due to the dicyclomine component's risk profile in young children.
- **Maximum**: Not established for this combination in young children.
- **Special Notes**: If used off-label in older children (>6-12 years) under strict medical supervision for severe spasms, single-ingredient products are preferred. The combination is typically for adolescents/adults.
### Adolescents (13-18 years)
- **Dose**: May follow adult dosing: **1 tablet** (Mefenamic Acid **250 mg** + Dicyclomine HCl **10 mg**).
- **Frequency**: Up to **3 times daily**.
- **Maximum**: **3 tablets/day** (Mefenamic Acid **750 mg**/day, Dicyclomine HCl **30 mg**/day).
- **Special Notes**: Consider weight; lower dose if significantly underweight.
## Safety Information
### Contraindications
- **Absolute**: Hypersensitivity to mefenamic acid, dicyclomine, or other NSAIDs (e.g., aspirin triad: asthma, rhinitis, nasal polyps).
- **Absolute**: **Infants < 6 months** (due to dicyclomine).
- **Absolute**: Active peptic ulcer disease, GI bleeding, inflammatory bowel disease.
- **Absolute**: Severe renal or hepatic impairment.
- **Absolute**: Obstructive uropathy, paralytic ileus, severe ulcerative colitis, glaucoma, myasthenia gravis.
- **Absolute**: History of coronary artery bypass graft (CABG) surgery (NSAID component).
- **Relative**: Cardiovascular disease, uncontrolled hypertension, asthma (non-NSAID induced).
### Common Adverse Effects
- **Very Common (>10%)**: Dry mouth (dicyclomine).
- **Common (1-10%)**: Nausea, vomiting, abdominal pain, diarrhea, constipation, dizziness, blurred vision (dicyclomine). Headache, heartburn (mefenamic acid).
- **Serious but Rare**: Gastrointestinal bleeding/perforation, acute kidney injury, severe allergic reactions (anaphylaxis), Stevens-Johnson syndrome, cardiovascular thrombotic events (NSAID). Respiratory depression, psychosis (dicyclomine overdose).
### Key Drug Interactions
- **Anticoagulants (e.g., Warfarin)**: Increased bleeding risk with Mefenamic Acid.
- **Lithium**: Increased lithium levels with Mefenamic Acid. Monitor levels.
- **Methotrexate**: Increased methotrexate toxicity. Avoid concomitant use.
- **Antihypertensives (e.g., ACE inhibitors, Diuretics)**: Reduced antihypertensive effect, increased renal toxicity risk with Mefenamic Acid.
- **Other Anticholinergics (e.g., TCAs, Antihistamines)**: Additive anticholinergic effects (dry mouth, blurred vision, urinary retention).
- **Corticosteroids**: Increased risk of GI adverse events (bleeding).
## Monitoring & Follow-up
- **Before Treatment**: Assess GI history, renal/hepatic function, blood pressure.
- **During Treatment**:
- Monitor for signs of GI bleeding (black stools, vomiting blood).
- Monitor renal function (creatinine, GFR) in patients at risk or with prolonged use.
- Monitor blood pressure periodically.
- Watch for changes in vision (blurred vision, increased intraocular pressure in glaucoma patients).
- Observe for urinary retention, especially in elderly or patients with prostate issues.
- **Clinical Signs**: Report persistent GI upset, unusual bleeding/bruising, blurred vision, difficulty urinating, or severe dizziness/confusion immediately.
## Clinical Pearls
- 💡 **Short-term Use**: Best used for acute, short-term relief of spasmodic pain due to NSAID and anticholinergic side effect profiles.
- 💡 **Take With Food**: To minimize gastrointestinal irritation and adverse effects.
- 💡 **Anticholinergic Effects**: Counsel patients about common anticholinergic effects like dry mouth, blurred vision, and constipation. Advise caution with driving.
- 💡 **Hydration**: Maintain adequate hydration to reduce the risk of renal adverse effects from Mefenamic Acid.
- 💡 **Pediatric Warning**: Emphasize this combination product is **not for infants** due to dicyclomine's serious risks.
> **⚠️ Important**: This information is for educational purposes only. Always consult current prescribing information, local guidelines, and clinical judgment before prescribing.