FDA records indicate that there are no current recalls for this drug.
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Questions & Answers
Side Effects & Adverse Reactions
For external use only
Do not use
- •
- if you are sensitive to Benzoyl Peroxide or have very sensitive skin. This product may cause irritation.
Ask a doctor or pharmacist before use
- •
- if you are using other topical acne drugs at the same time or right after use of this product. This may increase dryness, redness, or irritation of the skin. If this occurs, only one medication should be used unless a doctor directs otherwise.
When using this product
- •
- avoid contact with eyes. If contact occurs, flush thoroughly with water. Keep away from lips and mouth.
- •
- Avoid unnecessary sun exposure and use a sunscreen.
- •
- Avoid product contact with hair and dyed fabrics, including carpets and clothing which may be bleached by this product.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
For external use only
Do not use
- •
- if you are sensitive to Benzoyl Peroxide or have very sensitive skin. This product may cause irritation.
Ask a doctor or pharmacist before use
- •
- if you are using other topical acne drugs at the same time or right after use of this product. This may increase dryness, redness, or irritation of the skin. If this occurs, only one medication should be used unless a doctor directs otherwise.
Avoid contact with eyes. If contact occurs, flush thoroughly with water. Keep away from lips and mouth.
For external use only.
Do not use
- •
- If you are sensitive to Benzoyl Peroxide or have very sensitive skin. This product may cause irritation.
Ask a doctor or pharmacist before use.
- •
- If you are using other topical acne drugs at the same time or right after use of this product. This may increase dryness, redness, or irritation of the skin. If this occurs, only one medication should be used unless a doctor directs otherwise.
When using this product
- •
- Avoid contact with eyes. If contact occurs, flush thoroughly with water. Keep away from lips and mouth.
Avoid unnecessary sun exposure and use a sunscreen.
- •
- Avoid product contact with hair and dyed fabrics, including carpets and clothing which may be bleached by this product.
If excessive irritation occurs.
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
For the treatment of acne.
Apply only at night. Wait at least 10 minutes after applying Step 2 (until skin is dry), then use fingertips to massage into acne affected areas. Do not rinse off. For best results, do not use Retinol Complex at the same time as Step 3. Some mild tingling may occur and should be temporary until skin adjusts. Discontinue use if skin irritation develops or worsens.
For the treatment of acne.
History
There is currently no drug history available for this drug.
Other Information
There are no additional details available for this product.
Sources
Acnefree Clear Skin Treatments 24 Hour Severe Acne Clearing System Manufacturers
-
Valeant Pharmaceuticals North America Llc
Acnefree Clear Skin Treatments 24 Hour Severe Acne Clearing System | Mylan Institutional Inc.
BECAUSE OF THE UNIQUE PHARMACOKINETIC PROPERTIES, DIFFICULT DOSING SCHEDULE, AND SEVERITY OF THE SIDE EFFECTS IF PATIENTS ARE IMPROPERLY MONITORED, AMIODARONE HYDROCHLORIDE TABLETS SHOULD BE ADMINISTERED ONLY BY PHYSICIANS WHO ARE EXPERIENCED IN THE TREATMENT OF LIFE-THREATENING ARRHYTHMIAS WHO ARE THOROUGHLY FAMILIAR WITH THE RISKS AND BENEFITS OF AMIODARONE THERAPY, AND WHO HAVE ACCESS TO LABORATORY FACILITIES CAPABLE OF ADEQUATELY MONITORING THE EFFECTIVENESS AND SIDE EFFECTS OF TREATMENT.
In order to insure that an antiarrhythmic effect will be observed without waiting several months, loading doses are required. A uniform, optimal dosage schedule for administration of amiodarone hydrochloride tablets has not been determined. Because of the food effect on absorption, amiodarone hydrochloride tablets should be administered consistently with regard to meals (see CLINICAL PHARMACOLOGY). Individual patient titration is suggested according to the following guidelines:
For Life-Threatening Ventricular Arrhythmias, Such as Ventricular Fibrillation or Hemodynamically Unstable Ventricular TachycardiaClose monitoring of the patients is indicated during the loading phase, particularly until risk of recurrent ventricular tachycardia or fibrillation has abated. Because of the serious nature of the arrhythmia and the lack of predictable time course of effect, loading should be performed in a hospital setting. Loading doses of 800 to 1,600 mg/day are required for 1 to 3 weeks (occasionally longer) until initial therapeutic response occurs. (Administration of amiodarone hydrochloride tablets in divided doses with meals is suggested for total daily doses of 1,000 mg or higher, or when gastrointestinal intolerance occurs.) If side effects become excessive, the dose should be reduced. Elimination of recurrence of ventricular fibrillation and tachycardia usually occurs within 1 to 3 weeks, along with reduction in complex and total ventricular ectopic beats.
Since grapefruit juice is known to inhibit CYP3A4-mediated metabolism of oral amiodarone in the intestinal mucosa, resulting in increased plasma levels of amiodarone, grapefruit juice should not be taken during treatment with oral amiodarone (see PRECAUTIONS, Drug Interactions).
Upon starting amiodarone hydrochloride tablet therapy, an attempt should be made to gradually discontinue prior antiarrhythmic drugs (see PRECAUTIONS, Drug Interactions). When adequate arrhythmia control is achieved, or if side effects become prominent, amiodarone hydrochloride tablet dose should be reduced to 600 to 800 mg/day for one month and then to the maintenance dose, usually 400 mg/day (see CLINICAL PHARMACOLOGY, Monitoring Effectiveness). Some patients may require larger maintenance doses, up to 600 mg/day, and some can be controlled on lower doses. Amiodarone hydrochloride tablets may be administered as a single daily dose, or in patients with severe gastrointestinal intolerance, as a b.i.d. dose. In each patient, the chronic maintenance dose should be determined according to antiarrhythmic effect as assessed by symptoms, Holter recordings, and/or programmed electrical stimulation and by patient tolerance. Plasma concentrations may be helpful in evaluating nonresponsiveness or unexpectedly severe toxicity (see CLINICAL PHARMACOLOGY).
The lowest effective dose should be used to prevent the occurrence of side effects. In all instances, the physician must be guided by the severity of the individual patient’s arrhythmia and response to therapy.
When dosage adjustments are necessary, the patient should be closely monitored for an extended period of time because of the long and variable half-life of amiodarone and the difficulty in predicting the time required to attain a new steady-state level of drug. Dosage suggestions are summarized below:
Loading Dose
Adjustment and Maintenance Dose
(Daily)
(Daily)
Ventricular Arrhythmias
1 to 3 weeks
~1 month
usual maintenance
800 to 1,600 mg
600 to 800 mg
400 mg
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