Skip to main content

ARTEROLANE MALEATE

 ARTEROLANE MALEATE 


BRAND NAME:- no specific brand in single composition.



ARTEROLANE, also known as OZ277 or RBx 11160, is a substance that was tested for antimalarial activity. Its molecular structure is uncommon for pharmacological compounds in that it has both an ozonide (trioxolane) group and an adamantane substituent.

      

MECHANISM & PHARMACOLOGICAL ACTION:-   

ARTEROLANE acts rapidly at all stages of asexual schizogony  of malarial parasite including multidrug resistant P.f.,but has no effect on the hepatic stages. It accumulates in the food vacuole of the parasite,and thus differs from artemisinins which do not accumulates at this site. It also has moderate gametocidal activity similar to that of artemether - LUMEFANTRINE . 

Arterolane are well absorbed orally, and absorption is unaffected by food. Peak plasma arterolane concentration is reached 3-5 hours and it has a large volume of distribution . The major metabolic pathway is oxidation,Mainly  by CYP3A4 , which is also the primary ISOENZYME responsible for PIPERAQUINE metabolism . Arterolane is short acting and it's plasma t½ varies between 1-3 hours.


(It is a artemisinin based combination Therapy (ACT )  regimens for Uncomplicated falciparum malaria . )


IN  2012, RANBAXY OBTAINED APPROVAL TO MARKET THE ARTEROLANE/PIPERAQUINE COMBINATION DRUG IN INDIA, UNDER THE BRAND NAME SYNRIAM 


USED:- treatment of malaria 🦟.


SIDE EFFECTS:- 

mild headache, dizziness, vomiting, nausea, abdominal pain etc.


DOSE:- DIRECTION BY PHYSICIAN.

Comments

Popular posts from this blog

BOTULINUM TOXIN Uses, Side Effects, and More

 BOTULINUM TOXIN ( A or B ) BRAND NAME:- BOTOX ,DYSPORT  BOTULINUM TOXIN  A and B are highly potent exotoxins produced by Clostridium botulinum that are responsible for ' botulism' ( a type of food poisoning). These neurotoxic proteins cause long- lasting loss of cholinergic transmission by interacting with axonal proteins involved in exocytotic release of Ach. Localized injection of minute quantity of botulinum toxin.  PHARMACODYNAMIC :- Botulinum toxin A inhibits the release of acetylcholine, relieving muscle contraction and spasm associated with many conditions, such as incontinence and dystonia. Cosmetically, botulinum toxin A paralyses muscles in the face to temporarily treat wrinkles. The maximum effects of muscle paralysis occur four to seven days after a dose.When injected at therapeutic doses, botulinum toxin A causes partial chemical denervation of muscle tissue, causing local reduction of muscle activity. Muscle atrophy may result, axonal sprouting may beg...

Clonazepam used, Side effects, Dose, & more

Clonazepam  Brand name:- Lonazepam , Clonapax , Rivotril 0.5, 1.0, 2.0 mg tab. Clonazepam is a benzodiazepine. It works by increasing the action of a chemical messenger (GABA) which suppresses the abnormal and excessive activity of the nerve cells in the brain. Pharmacodynamic:- The pharmacodynamic properties of clonazepam are common among benzodiazepines and include anticonvulsive, sedative, muscle relaxing and anxiolytic effects . Animal data and electroencephalographic investigations in man have shown that clonazepam rapidly suppresses many types of paroxysmal activity including the spike and wave discharge in absence seizures (petit mal), slow spike wave, generalized spike wave, spikes with temporal or other locations, as well as irregular spikes and waves Label . Moreover, the agent can also decrease the frequency, amplitude, duration, and spread of discharge in minor motor seizures Label . Generalized EEG abnormalities are more readily suppressed by clonazepam than are focal ...

CLOMIPHENE CITRATE Uses, Side Effects, and More

 CLOMIPHENE CITRATE BRAND NAME:- CLOMIPHENE, FERTOMED, CLOFERT, CLOME 25,50,100mg tab.  Clomiphene is a selective estrogen receptor modulator (SERM) which treats female infertility. It works by promoting the release of reproductive hormones. This helps stimulate the release of eggs from the ovary (ovulation). PHARMACODYANIMCS:- Clomifene (previously clomiphene) is an orally administered, non steroidal, ovulatory stimulant that acts as a selective estrogen receptor modulator (SERM). Clomifene can lead to multiple ovulation, and hence increase the risk of conceiving twins. In comparison to purified FSH, the rate of ovarian hyperstimulation syndrome is low. There may be an increased risk of ovarian cancer and weight gain. Clomifene is capable of interacting with estrogen-receptor-containing tissues, including the hypothalamus, pituitary, ovary, endometrium, vagina, and cervix. It may compete with estrogen for estrogen-receptor-binding sites and may delay replenishment of intracel...