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Atromid-S

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Atromid-S

Discontinued Warning IconPlease Note: This Brand Name drug is no longer available in the US.
(Generic versions may still be available.)

Atromid-S Side Effects Center

Medical Editor: John P. Cunha, DO, FACOEP

Atromid-S (clofibrate capsules) is an antilipidemic drug used to lower high levels of cholesterol (a type of fat) in the blood. It is especially good at lowering triglycerides and very-low-density lipoprotein (VLDL) (a form of cholesterol). The brand name of this medication is discontinued, but generic versions may be available. Common side effects include bloating, flatulence, nausea, vomiting, diarrhea, headache, dizziness, drowsiness, or impotence.

The recommended dosage of Atromid-S for adults is 2 g daily in divided doses. Atromid-S may interact with anticoagulants, insulin or oral diabetes medications, or other cholesterol-lowering drugs. Tell your doctor all medications and supplements you use. Atromid-S may pass into the system of a fetus and can build up dangerously in unborn babies, who do not yet have the ability to break down and pass this drug from the body. Tell your doctor if you are pregnant before taking Atromid-S. This drug passes into breast milk. Since babies do not yet have the ability to break down this drug, a dangerous buildup could occur. Consult your doctor before breastfeeding.

Our Atromid-S (clofibrate capsules) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What is Patient Information in Detail?

Easy-to-read and understand detailed drug information and pill images for the patient or caregiver from Cerner Multum.

Atromid-S in Detail - Patient Information: Side Effects

If you experience any of the following serious side effects, stop taking clofibrate and seek emergency medical attention:

  • an allergic reaction (difficulty breathing; closing of your throat; swelling of your lips, tongue, or face; or hives);
  • chest pain or an irregular heart beat;
  • severe stomach pain with nausea and vomiting;
  • fever and chills, a sore throat, or a flu-like feeling;
  • blood in your urine or a decrease in urination;
  • swelling of your ankles or legs;
  • muscle cramps, muscle weakness, muscle aches, or muscle pain;
  • joint pain; or
  • sudden weight gain.

Other, less serious side effects may be more likely to occur. Continue to take clofibrate and talk to your doctor if you experience

  • bloating or flatulence;
  • nausea, vomiting, or diarrhea;
  • headache;
  • dizziness or drowsiness; or
  • impotence.

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

Read the entire detailed patient monograph for Atromid-S (Clofibrate) »

What is Prescribing information?

The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.

Atromid-S FDA Prescribing Information: Side Effects
(Adverse Reactions)

SIDE EFFECTS

The most common is nausea. Less frequently encountered gastrointestinal reactions are vomiting, loose stools, dyspepsia, flatulence, and abdominal distress. Reactions reported less often than gastrointestinal ones are headache, dizziness, and fatigue; muscle cramping, aching, and weakness; skin rash, urticaria, and pruritus; dry brittle hair, and alopecia.

The following reported adverse reactions are listed alphabetically by systems:

Cardiovascular

Increased or decreased angina.

Cardiac arrhythmias.

Both swelling and phlebitis at site of xanthomas.

Dermatologic

Allergic reactions including urticaria.

Skin rash.

Pruritus.

Dry skin and dry, brittle hair.

Alopecia.

Toxic epidermal necrolysis.

Erythema multiforme.

Stevens-Johnson syndrome.

Gastrointestinal

Gallstones.

Nausea.

Vomiting.

Diarrhea.

Gastrointestinal upset (bloating, flatulence, abdominal distress).

Hepatomegaly (not associated with hepatotoxicity).

Stomatitis and gastritis.

Genitourinary

Findings consistent with renal dysfunction as evidenced by dysuria, hematuria, proteinuria, decreased urine output. One patient's renal biopsy suggested "allergic reaction."

Impotence and decreased libido.

Hematologic

Leukopenia.

Potentiation of anticoagulant effect.

Anemia.

Eosinophilia.

Agranulocytosis.

Musculoskeletal

Myalgia (muscle cramping, aching, weakness).

"Flu-like" symptoms.

Myositis.

Myopathy.

Rhabdomyolysis in the setting of preexisting renal insufficiency.

Arthralgia.

Neurologic

Fatigue, weakness, drowsiness.

Dizziness.

Headache.

Miscellaneous

Weight gain.

Polyphagia.

Laboratory Findings

Abnormal liver-function tests as evidenced by increased transaminase (SGOT and SGPT), BSP retention, and increased thymol turbidity.

Proteinuria.

Increased creatine phosphokinase.

Hyperkalemia in association with renal insufficiency and continuous ambulatory peritoneal dialysis treatment.

Reported adverse reactions whose direct relationship with the drug has not been established: peptic ulcer, gastrointestinal hemorrhage, rheumatoid arthritis, tremors, increased perspiration, systemic lupus erythematosus, blurred vision, gynecomastia, thrombocytopenic purpura.

Read the entire FDA prescribing information for Atromid-S (Clofibrate) »

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Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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