Alfamec

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Alfamec

Medically reviewed

Marina Burgos

Last updated on 10/01/2026

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Alfamec

Property Description
Active Ingredient Ivermectin
Pharmacological Class Antiparasitic agent (Endectocide)
Origin Semisynthetic (Derived from macrocyclic lactones)
Primary Forms Solution for Injection (Veterinary), Tablets, Topical Preparations
General Purpose Control of internal and external parasitic infestations

Defining the Medicinal Entity and Its Position

Alfamec is a prescription medicine that utilizes the compound Ivermectin as its sole active ingredient. It is broadly classified as an endectocide, a specialized type of antiparasitic agent that is effective against both internal parasitic worms and external arthropods (mites and lice). This dual functionality defines its primary purpose: the control and elimination of a wide variety of parasitic infestations.

Composition and Origin: The Active Ingredient's Nature

The chemical core of Alfamec is Ivermectin, a semisynthetic compound belonging to the avermectins, which are potent macrocyclic lactones. Its foundation originates from the fermentation products of the soil bacterium Streptomyces avermitilis. Pharmacological studies have clinically recognized Ivermectin for its high efficacy and broad spectrum of activity against numerous parasitic agents. The medicine is a single-ingredient product, available across multiple high-level dosage forms, including tablets, topical applications, and solutions for injection.

How Ivermectin Works (Mechanism Principle)

The efficacy of Alfamec stems from Ivermectin's highly selective mechanism that targets the parasite's nervous system. The substance acts by selectively binding to glutamate-gated chloride ion channels found in the nerve and muscle cells of susceptible invertebrates. This binding disrupts neurosynaptic transmission, leading to the rapid and irreversible paralysis and subsequent death of the parasitic organism. This targeted action is generally distinct from major neurological pathways in mammalian hosts, forming the basis for its therapeutic selectivity.

Regulatory References

  1. Ivermectin: MedlinePlus Drug Information

What side effects are possible with Alfamec?

Possible Side Effects and Safety Information

This section details the officially documented adverse effects and safety constraints of Alfamec (Ivermectin), based strictly on regulatory documents from government health authorities (e.g., FDA, EMA).

Adverse Reaction Category Official Documentation Summary
Common / More Common Reactions Headache, dizziness, nausea, diarrhea, abdominal pain, fatigue, fever, asthenia, rash, pruritus (itching), and myalgia (muscle pain). These are often associated with the body's reaction to the dying parasites, particularly known as the Mazzotti reaction in Onchocerciasis treatment.
System-Organ Classes Involved Adverse reactions are formally documented across several systems, including Nervous System Disorders (e.g., somnolence, confusion, seizures, tremor), Gastrointestinal Disorders, Skin and Subcutaneous Tissue Disorders, and Ocular Disorders (e.g., eyelid edema, conjunctivitis).
Serious Adverse Reactions Serious or fatal Encephalopathy is reported rarely, primarily in patients treated for Onchocerciasis who have a heavy co-infection with the parasite Loa loa. Post-marketing reports also include severe cutaneous reactions, such as Stevens-Johnson Syndrome (SJS) and Toxic Epidermal Necrolysis (TEN).

Population-Specific Safety Constraints

  • Pediatric Use: Safety and effectiveness have not been established in pediatric patients weighing less than 15 kg.
  • Pregnancy and Lactation: Use during pregnancy and lactation requires careful evaluation, as safety has not been fully established, and the drug is excreted in human milk in low concentrations.
  • Loa loa Co-infection: Patients heavily infected with Loa loa are at an increased risk of serious neurological events, including encephalopathy.

Other Regulatory Safety Notes

  • Temporal Pattern: Adverse experiences related to the Mazzotti reaction are typically common during the first three days after treatment.
  • Contraindication: The medicine is contraindicated in individuals with a known hypersensitivity to the active substance or any component of the product.
  • Drug Interaction Note: Post-marketing reports have rarely noted an increased International Normalized Ratio (INR) when Ivermectin was co-administered with Warfarin.

Overdose and Emergency Response

Overdose and When to Seek Help

Overdose of Alfamec (Ivermectin) has been officially associated with specific clinical manifestations and potentially severe outcomes. The official guidance from government health bodies mandates immediate action if an overdose is suspected.

Documented Overdose Manifestations

Symptoms reported following high-dose exposure or overdose primarily involve the gastrointestinal and nervous systems:

  • Gastrointestinal: Nausea, vomiting, diarrhea, and abdominal pain.
  • Neurological: Decreased consciousness, confusion, severe sleepiness/drowsiness, hallucinations, headache, dizziness, and loss of coordination (ataxia).
  • Other Effects: Rash, hives, swelling, and general weakness.

Severe Outcomes and Emergency Actions

Regulators have documented that severe exposure is associated with life-threatening effects, including seizures, coma, low blood pressure (hypotension), and fast heart rate (tachycardia). Fatal outcomes have been reported in connection with overdose.

Urgent Help-Seeking is Required

If any symptoms of toxicity occur or overdose is suspected, immediate medical attention must be sought. Official sources advise calling the national Poison Help line for advice. For life-threatening signs, such as collapse, seizure, trouble breathing, or inability to be awakened, emergency services must be called immediately.

Management and Antidote Status

Alfamec has no specific antidote documented in official labeling. Management is supportive and symptomatic, focusing on controlling severe clinical signs and preventing further absorption. Procedural steps like gastric lavage may be considered for large ingestions.

Therapeutic Uses of Alfamec

What Alfamec Treats: Main Uses and Benefits

Alfamec (Ivermectin) is considered relevant for managing parasitic infections in patients. This medication is commonly used to help address infections caused by various parasitic worms, such as Strongyloidiasis and the microfilarial stage of Onchocerciasis (River Blindness). It is also considered relevant for managing external parasitic infestations, including pervasive conditions like Scabies and common issues like Head Lice, as well as being applied to help address the burden of persistent papules and pustules seen in conditions like Rosacea.

In clinical settings, Alfamec is applied in clinical settings that involve acute or unstable symptom patterns, and may assist with managing symptoms linked to organ-specific functional stress. In these contexts, the medication provides supportive relief when symptoms interfere with routine activities.

“It is used to help address symptom clusters that may become intense or disruptive, contributing to improved comfort during symptomatic periods.”

Quick Fact: Addresses Symptoms Related to Persistent Pruritus and Intestinal Distress

The medication is applied in addressing severe dermatological symptoms linked to infestation, such as debilitating pruritus, thereby contributing to easing the overall symptom load. This approach supports the patient during episodes of heightened discomfort and assists with maintaining functional stability across various parasitic and inflammatory skin conditions.

Regulatory References

  1. NIH MedlinePlus Drug Information

Eligibility and Restrictions for Use

The eligibility for Alfamec (Ivermectin) is strictly governed by regulatory documentation, defining specific groups who may be treated and those who are excluded or require caution.

Populations for Whom Use is Prohibited or Restricted

Category Official Regulatory Status (Ivermectin Tablets)
Absolute Contraindication Patients with a known hypersensitivity or allergy to Ivermectin or any component of the formulation.
Age-Related Restriction Safety and effectiveness have not been established in pediatric patients weighing less than 15 kg (33 lbs).
Pregnancy Use is not recommended during pregnancy as safety has not been established.
Conditional Use Patients with a history of residence in Loa loa-endemic areas must undergo pretreatment assessment due to the rare risk of a serious adverse reaction.
Lactation Treatment of nursing mothers should only be undertaken when the risk of delayed treatment to the mother outweighs the possible risk to the newborn, as the drug is found in human milk.
Geriatric Caution Older adults are generally eligible, but caution is recommended due to the greater frequency of age-related hepatic, renal, or cardiac dysfunction.

Eligibility is established for adults and children who meet the minimum weight threshold of 15 kg, provided they have no documented hypersensitivity to the product. Use is limited or conditional for patients with specific comorbidities or life-stage statuses, such as pregnancy or Loa loa co-infection, as explicitly defined in the regulatory labeling.

What should I know about interactions with other medicines?

Alfamec is a combination medicine typically containing pregabalin and methylcobalamin (Vitamin B12). The interactions noted for this product are primarily related to the pregabalin component, which acts as a central nervous system (CNS) depressant.

Documented Drug-Drug Interactions

The most significant concern for Alfamec involves co-administration with other substances that also depress the central nervous system. This combination can lead to enhanced sedative effects, increasing the risk of somnolence, dizziness, and respiratory depression.

  • CNS Depressants: This category includes medicines such as opioids (narcotic pain relievers), benzodiazepines (for anxiety or sleep), and barbiturates. Combining Alfamec with these agents may necessitate careful medical oversight and dosage adjustments.
  • Thiazolidinedione Antidiabetic Agents: Using Alfamec alongside this class of medicines for diabetes may increase the risk of fluid retention and weight gain. Patients with underlying heart conditions should be monitored closely for potential worsening of heart complications.

Other Interaction Contexts

  • Alcohol: Consumption of alcohol is strongly advised against while taking Alfamec, as it can significantly enhance the drug’s depressive effects on the CNS, leading to excessive drowsiness and impaired coordination. This combination increases the risk of accidental injury.
  • Antacids: Some formulations of Alfamec containing additional components may have absorption decreased by antacids, suggesting a potential need to space administration times.
  • Orlistat: This weight-loss medication may reduce the absorption of pregabalin, potentially decreasing its effectiveness, and increasing the risk of convulsions. Close monitoring may be required.

Mechanism of Action

Alfamec's action is defined by a highly selective mechanism directed at the unique physiology of susceptible parasites. The molecular action centers on binding to the parasite's glutamate-gated chloride channels ( GluClRs). The drug acts as an agonist, forcing the continuous opening of these channels, which results in a substantial and persistent influx of chloride ions into the nerve and muscle cells. This ion flux leads to cellular hyperpolarization, effectively silencing all neural and muscle activity. This rapid shutdown of signaling pathways culminates in severe, systemic flaccid paralysis across the entire organism, including the inability to move or feed, thereby shaping the resulting physiological consequences. The mechanism exhibits high selectivity due to the primary targets being absent in mammals and the host's protective P-glycoprotein efflux system limiting drug penetration into the mammalian CNS. This specificity, however, imposes constraints, as the mechanism does not apply to parasites like flukes and tapeworms, which lack the susceptible GluClR subtype.

Dosage and Administration Information

Alfamec (ivermectin) is an antiparasitic agent indicated for the treatment of certain infections, such as intestinal strongyloidiasis and onchocerciasis (river blindness). It is crucial to follow the prescription exactly as provided by your healthcare professional. Do not use more, less, or for a longer duration than instructed.

Administration

Alfamec oral tablets are typically taken as a single dose with water on an empty stomach (no food within two hours before or after the dose). The specific dose is determined by the patient’s body weight and the condition being treated. For children under six years of age, the tablets may need to be crushed before swallowing.


Dosage Guidelines (Oral Tablets)

The number of 3 mg tablets to be taken in a single dose depends on the patient's weight for the two primary indications:

Body Weight (kg) Strongyloidiasis (200 mug/kg) Onchocerciasis (150 mug/kg)
15–24 kg 1 tablet 1 tablet
25–35 kg 2 tablets 2 tablets
36–50 kg 3 tablets 3 tablets
51–65 kg 4 tablets 4 tablets
66–84 kg 5 tablets 4 tablets
ge 85 kg Calculated based on 200 mug/kg Calculated based on 150 mug/kg

Note: This table provides general guidance. Your prescribed dose may differ based on your medical condition. Repeat dosing, such as every 3 to 12 months for Onchocerciasis, may be necessary to control the infection.


Post-Treatment

For strongyloidiasis, follow-up stool examinations are generally required after treatment to confirm the eradication of the infection. Do not take a second dose without consulting your doctor, even if symptoms persist, as recovery from some conditions may not be fully evident for several weeks.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Alfamec

Research Evidence for Strongyloidiasis and Onchocerciasis

The research into Ivermectin for parasitic worm infections, such as Strongyloidiasis and Onchocerciasis (River Blindness), includes data from Randomized Controlled Trials (RCTs) and large-scale, long-term epidemiological studies. For Strongyloidiasis, trials were conducted to compare treatment regimens and research examined outcomes related to parasitological clearance, measuring if the parasite could still be detected after treatment. Studies was evaluated in adults and children, and research highlights changes measured in the short-term, typically within 90 days.

For Onchocerciasis, the evidence was studied for its impact on community-level disease indicators, primarily by monitoring the reduction of microfilariae load. Large treatment programs were observed in endemic areas over long periods to observe indicators related to disease transmission and monitoring of long-term ocular measures. What remains uncertain for Strongyloidiasis is the optimal dosing plan to confirm complete and sustained clearance of the parasite. Research is ongoing because the treatment targets only the larval stage, meaning studies must continue over many years to address the life cycle of the adult worm.


Studies on External Infestations: Scabies and Head Lice

For external infestations like Scabies, research was evaluated in a variety of short-term RCTs, often comparing oral Ivermectin to other topical treatments. Studies explored clinical outcomes related to physical discomfort, focusing on achieving clinical cure and the resolution of severe itching (pruritus). Findings describe patterns observed in the studies where clinical cure was associated with the treatment regimen.

Evidence for Head Lice (Pediculosis) is limited and often was observed in some studies with smaller patient groups. These trials research examined the eradication of both adult lice and their eggs. Research limitation frames for Scabies include that variability remains in the comparative evidence regarding single-dose versus multi-dose regimens. For Head Lice, the evidence quality varies across studies, and more definitive, large-scale comparative evidence is lacking.

Key Studies & References

  1. Ivermectin in the management of scabies: a systematic review

Frequently Asked Questions (FAQ)

Common questions about Alfamec (FAQ)

Q: How quickly should I expect to feel a difference after starting Alfamec?

Studies and official product information indicate that adverse reactions associated with the parasite die-off—such as the Mazzotti reaction—typically begin within the first three days of treatment. However, the time it takes for infection symptoms to fully resolve can vary. For certain infections, full resolution of symptoms may not be evident for several weeks.


Q: Does Alfamec interact with common pain relievers like ibuprofen or acetaminophen?

Regulatory documents do not list any major or moderate drug interactions between the active ingredient in Alfamec and common non-opioid pain relievers such as ibuprofen or acetaminophen. It is important to inform your healthcare provider about all over-the-counter medicines being taken.


Q: Can a person take Alfamec if they are already on blood pressure medication?

Official labeling contains no general contraindication for taking Alfamec with blood pressure medications. However, the drug has been rarely reported to increase the effect of the blood thinner Warfarin, which is sometimes used by patients with heart conditions. Patients are advised to inform their physician about all prescription drugs being taken, including blood pressure medications.


Q: Does Alfamec affect sleep patterns, like causing drowsiness or insomnia?

Yes, official regulatory documents list somnolence (drowsiness or sleepiness) and confusion as reported adverse reactions. Awareness of these effects is important when performing activities that require concentration.


Q: What should I do if a potential side effect from Alfamec seems concerning, but not severe?

Official product information suggests contacting a healthcare provider to report any side effects. You can also report side effects directly to the relevant regulatory authority. This guidance applies to all adverse reactions, regardless of how severe they feel.


Q: How long does Alfamec stay in your system after stopping the medication?

According to official pharmacokinetic data, the plasma half-life of the active ingredient is approximately 18 hours after administration. The drug and its breakdown products are then primarily eliminated through the feces, typically over a period of about 12 days.


Q: Is there a generic version of Alfamec available?

Yes, Alfamec's active ingredient, Ivermectin, is available as an FDA-approved generic oral tablet from various manufacturers. Generic versions contain the same active ingredient and are approved by regulatory bodies, such as the FDA.


Q: Does Alfamec interfere with common lab test results?

The medicine is generally not known to interfere with routine laboratory tests. However, post-marketing reports have rarely noted that taking this medicine with Warfarin may be associated with an increase in the International Normalized Ratio (INR), a test used to measure blood clotting time.


Q: Is it okay to take Alfamec with a glass of milk?

Official administration instructions specify that the tablets should be taken with water on an empty stomach. This includes avoiding food and substances like milk within the specified time frame, as taking the drug with a high-fat meal can significantly increase its absorption.


Q: Can a patient drive or operate machinery while taking Alfamec?

Official product labeling documents potential side effects such as dizziness and somnolence (drowsiness). Awareness of these potential effects on coordination and attention is important before engaging in activities like driving or operating machinery.


Q: How does Alfamec work at a basic level inside the body?

The medicine's mechanism of action targets the parasite's nerve and muscle cells. It works by causing a rapid and irreversible paralysis of the parasitic organism, leading to its death and eventual elimination from the body.


Q: Is Alfamec considered a long-term or short-term treatment?

The treatment is primarily considered short-term, as the initial administration is often a single oral dose for most infections. For certain conditions like Onchocerciasis, repeat dosing may be necessary intermittently, such as every 3 to 12 months, which constitutes a long-term management strategy.


Q: Can Alfamec cause changes in mood or anxiety levels?

While the official labeling documents neurological effects such as confusion, and rarely, more serious events like seizures or encephalopathy, changes specifically labeled as 'mood' or 'anxiety' are not included in the standard list of reported adverse reactions.


Q: Do any herbal supplements commonly interact with Alfamec?

Specific interactions with herbal supplements are not generally listed in the regulatory documents. Official product information emphasizes the importance of informing the healthcare provider about all medicines, vitamins, and herbal products being taken.


Q: Is Alfamec a medication that needs to be tapered off, or can it be stopped immediately?

Based on its primary use, the medicine is typically administered as a single dose. A scheduled tapering (gradual reduction of the dose) is generally not necessary upon completion of treatment.


Q: What are the signs that Alfamec might not be working for a patient?

For infections like Strongyloidiasis, follow-up tests, such as stool examinations, are often required to confirm the parasite has been eliminated. In all cases, patients are advised to report to their healthcare provider if symptoms persist or fail to improve after treatment.


Q: Can Alfamec affect fertility?

Studies conducted in animal models, specifically rats, found that the active ingredient in Alfamec had no adverse effects on fertility. This finding was observed even at doses higher than the maximum recommended human dose.


Q: Do lifestyle factors, like smoking or heavy alcohol use, affect how Alfamec works?

Official labeling strongly advises against alcohol consumption, as it can enhance the drug’s effects and increase the risk of side effects like dizziness and somnolence. The labeling does not specifically address how smoking may affect the drug’s function.


Q: What does 'bioavailability' mean in the context of the Alfamec pill?

Bioavailability is a pharmacokinetic term that refers to the amount of the drug that successfully enters the bloodstream and becomes available to act on the body. Regulatory documents note that taking the pill with food can significantly increase its bioavailability, which is why it is directed to be taken on an empty stomach.

How should Alfamec be stored and disposed of?

Official Storage and Disposal Requirements

Regulatory documentation establishes mandatory storage conditions for Alfamec, differentiating between the unopened and opened container states to ensure stability.

Storage Condition Unopened Vial Opened Vial (In-Use)
Temperature Store below 25 C Store at 2 - 8 C (refrigerated)
Freezing/Refrigeration Do not refrigerate or freeze Do not freeze
Stability Period Until expiry date (EXP) 28 days

All vials must be kept protected from light. It is required to keep Alfamec out of the sight and reach of children. The disposal of any unused product or waste material must be carried out in accordance with all applicable local requirements for pharmaceutical waste.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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