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Albenzole (Albendazole)

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Albenzole is a medication used for the treatment of a variety of parasitic worm infestations. It is useful for giardiasis, trichuriasis, filariasis, neurocysticercosis, hydatid disease, pinworm disease, and ascariasis, among other diseases. It is taken orally.

Other names for this medication:
Ablaze, Albazio, Albendazole, Albex, Alenda, Alzole, Anoworm, Antiworm, Arezole, Bendex, Benzola, Beworm, Byeworm, Combantrin, Dabdesyre, Dispel, Elbenol, Foxnill, Gallab, Mbend, Mebzol, Midazole, Nbworm, Nemaban, Nubend, Pedazole, Tiveable, Trualba, Wocid, Wormazan, Wormis, Wormja, Wormkut, Worzole, Zantol

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Also known as: Albendazole


The target of Generic Albenzole is struggle against certain tapeworm infections. Generic Albenzole is acting by killing sensitive parasites. It is an anthelmintic. Generic name of Generic Albenzole is Albendazole. Albenzole is also known as Albendazol, Albex, Alminth, Helmidazole, Eskazole, Zentel. Brand name of Generic Albenzole is Albenzole.


If you have trouble swallowing the tablet whole, it may be crushed or chewed with a little water. Take Generic Albenzole tablets orally with food. Take Generic Albenzole at the same time with water. If you want to achieve most effective results do not stop taking Generic Albenzole suddenly.


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.


Store at room temperature between 20 and 25 degrees C (68 and 77 degrees F) away from moisture and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Albenzole 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.


Avoid being near people who are sick or have infections. Tell your doctor at once if you develop signs of infection.

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The Dsc complex binds SREBP and cleavage requires components of the ubiquitin-proteasome pathway: the E2-conjugating enzyme Ubc4, the Dsc1 RING E3 ligase, and the proteasome. Development of bone-like substance in cartilaginous rat nasal septum under experimental conditions. Standardized mean differences were pooled for health-related quality of life and performance-based outcomes. These findings with PC12 cells suggest that staurosporine might act downstream from K252a and NGF on components of one or more signal transduction pathways by which NGF selectively affects the expression of certain traits. An exotherm of eutectic crystallization of NaCl was occasionally observed at -37 degree C, with a higher probability of formation at 150 mM extraliposomal NaCl than at 50 mM.

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Joint care: the seeds of support are sown and the harvest is strength. Further in vivo studies revealed that NMB04 possessed more potent inhibitory activity against human Blys as compared to an existing antibody, Belimumab. HTS identifies novel and specific uncompetitive inhibitors of the two-component NS2B-NS3 proteinase of West Nile virus. In order to verify the genetic basis of this variation, the DR B exon-2 of the major histocompatibility locus, known for coding the antigen recognition site, from the Hallikar breed of Indian cattle was amplified by PCR, cloned and sequenced. We found that anti-VEGF monotherapy is more effective on the recovery of visual acuity than combination therapy and more researches with lager sample size should be performed to study on the effect of the two therapy approaches on CRT and number of injections. Open surgical treatment included direct clipping, trapping, or wrapping and interventional treatment included stent-assisted coiling or simple stent placement. When human dental pulp cells were stimulated by the inflammatory cytokine tumor necrosis factor-alpha (TNF-alpha), PA activity in the conditioned medium was increased, indicating that TNF-alpha provoked PA secretion. Assessment of Cortical Dysfunction in Patients with Intermittent Exotropia: An fMRI Study. Groups of 5 male and 5 female CD rats were exposed 6 h/d, 5 d/wk for 4 wk to either TECP or PCP at target concentrations of 0, 100, 300, 600, or 900 ppm (single exposure only).

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