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Acniriv (Adapalene)

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Acniriv is used to treat acne. It may decrease the number and severity of acne pimples and promote quick healing of pimples that do develop. Acniriv belongs to a class of medications called retinoids. It works by affecting the growth of cells and decreasing swelling and inflammation.

Other names for this medication:
Aclene, Acneril, Acneris, Acniriv, Acnovate, Adaferin, Adapalene, Adapen, Adaple, Adaret, Adgraze, Adiff, Adina, Aditop, Adlene, Alangel, Apalene, Apgel, Clinred, Daple, Deriva, Difra, Edplin, Faceclin, Labopene, Medapine, Rozac, Soflene, Vandep, Zolvee

Similar Products:
Depakote, Bactrim, Fosamax, Eulexin, Nuvigil

Also known as: Adapalene


Acniriv is a third-generation topical retinoid primarily used in the treatment of acne. Acniriv is a gel used for the treatment of acne (blackheads, whiteheads and pimples) of the face, chest or back. Acniriv gel is a clear gel that powers deep inside your pores to control the buildup that leads to acne. It helps prevent the formation of new acne lesions, and can also help get rid of lesions already present. Acniriv works under the skin surface to unclog pores and clear up pimples. Acniriv is also known as Adapalene, Adapen, Adaferin. Generic name of Acniriv is Adapalene.


Follow the directions for using this medicine provided by your doctor. Use Acniriv exactly as directed. Acniriv is best applied after washing and drying your skin. Apply a thin layer of gel to the affected areas once daily at bedtime. Avoid the eyes, lips and nose. Do not allow this preparation to come into contact with the mucous membranes (e.g. mouth, vagina, inside of nose etc.). Try not to touch the treated areas overnight. Do not use any harsh soaps or exfoliants while you are being treated with Acniriv. Acniriv should not be used on broken, sunburnt or infected skin. You may notice a slight change of colour of the skin you are applying this preparation to. This is only temporary and should return to normal soon after finishing treatment with Acniriv. Continue using Acniriv until no new acne spots appear. You may need to use it for several months. You should notice some clinical improvement after 4-8 weeks and more improvement after further use. There may be a worsening of acne during the first few weeks of therapy because Acniriv promotes the growth of pimples that have begun to form but are not yet visible. Therefore, treatment should not be stopped if acne appears to be worsening. Use a sunscreen cream and wear protective clothing if exposure to strong or prolonged sunlight cannot be avoided. Weather extremes such as wind or cold may also be irritating.


Seek emergency medical attention if you think you have used too much of this medicine. Overdose symptoms may include skin redness, scaling, or irritation.


Store at a room temperature between 20 and 25 degrees C (68 and 77 degrees F) away from moisture, light and heat. Throw away the after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Acniriv are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


You should not use Acniriv if you are allergic to adapalene.

Ask a doctor or pharmacist if it is safe for you to use this medicine if you have other medical conditions.

It is not known whether adapalene passes into breast milk or if it could harm a nursing baby. Do not use this medicine without a doctor's advice if you are breast-feeding a baby.

It is not known whether Acniriv will harm an unborn baby. Do not use this medicine without a doctor's advice if you are pregnant.

Acniriv is not approved for use by anyone younger than 12 years old.

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In vitro and ex vivo inhibition of hepatitis A virus 3C proteinase by a peptidyl monofluoromethyl ketone. Changes of pulmonary and cardiovascular functions in subjects confined intermittently in a low-pressure chamber for 3 consecutive days. Urinary steroids and plasma components of the renin-angiotensin system (RAS) were measured using specific radioimmunoassays. US examination does not allow to differentiate between vocal cord paralysis and their immobilization. The favorable responses to interferon-alpha therapy in these two cases suggest that this is an effective and well-tolerated treatment for lymphangiomas in children. T-DMRs are located in not only genic but also nongenic regions-including transposable genetic elements, such as short interspersed transposable element. Lactic and succinic dehydrogenase activity in nitrite toxicosis in the guinea pig. In concordance with this suggestion, we found that the Tof1/Csm3/Mrc1 checkpoint complex interacts directly with the MCM helicase during both replication fork progression and when the replication fork is stalled. Addition of the tag serves to increase the yield of the protein as well as to ensure a homogeneous protein product following tag cleavage. Mirroring maturational processes on the cellular level, DWI has to be regarded as a morphological method as well as a functional instrument, giving insight into molecular processes during the formation of axons and myelin sheets and into the steric arrangement of white matter tracts the formation of which is strongly influenced by their function.

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Combined 111In WBC/99mTc sulfur colloid marrow images improve the specificity for detection of osteomyelitis in regions containing active bone marrow. O-linked N-acetylglucosamine (O-GlcNAc) is a ubiquitous nucleocytoplasmic protein modification that has a complex interplay with phosphorylation on cytoskeletal proteins, signaling proteins and transcription factors. We report a case of spontaneous rupture of the spleen and liver in a patient on warfarin therapy for deep venous thrombosis. Comparison of isotope ratio mass spectrometry and nondispersive isotope-selective infrared spectroscopy for 13C-urea breath test. The development of limit dextrinase activity during the germination of cereals. Despite its nonspecificity, ability to modify DNA and multiple molecular modes of action, NAC has therapeutic value for reducing endothelial dysfunction, inflammation, fibrosis, invasion, cartilage erosion, acetaminophen detoxification and transplant prolongation. The timespan between baseline and interim was on average 15 months and the period between interim and final examination averaged 16 months.

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