Risedronic acid

Risedronic acid
Systematic (IUPAC) name
(1-hydroxy-1-phosphono-2-pyridin-3-yl-ethyl)phosphonic acid
Clinical data
AHFS/Drugs.com International Drug Names
Pregnancy
category
  • AU: B3
  • US: C (Risk not ruled out)
Routes of
administration		 Oral
Legal status
Legal status
Pharmacokinetic data
Bioavailability 0.63%
Protein binding ~24%
Metabolism None
Biological half-life 1.5 h
Excretion Renal and fecal
Identifiers
CAS Number 105462-24-6 YesY
ATC code M05BA07 (WHO)
PubChem CID 5245
IUPHAR/BPS 3176
DrugBank DB00884 N
ChemSpider 5055 N
UNII KM2Z91756Z N
ChEMBL CHEMBL923 N
Chemical data
Formula C7H11NO7P2
Molar mass 283.112 g/mol
 NYesY (what is this?)  (verify)

Risedronic acid (INN) often used as its sodium salt risedronate sodium (USAN) is a bisphosphonate used to strengthen bone, treat or prevent osteoporosis, and treat Paget's disease of bone. It is produced and marketed by Warner Chilcott, Sanofi-Aventis, and in Japan by Takeda under the trade names Actonel, Atelvia, and Benet. It is also available in a preparation that includes a calcium carbonate supplement, as Actonel with Calcium.

Administration

Risedronate is taken orally, usually weekly or monthly. Notably, if risedronate lodges in the esophagus, it can lead to esophageal ulcers. Therefore, it is recommended that risedronate be taken with the body upright, and followed by a glass of water. Moreover, risedronate is poorly absorbed when taken with food, so it is recommended that no food or drink other than water be taken for 2 hours before and 30 minutes after taking risedronate. Risedronate has a faster esophageal transit time and different chemical chain which results in less gastrointestinal side-effects than other drugs in this class. The dosage instructions also show that risedronate can be taken with less water than other drugs in the class. Risedronate is also available as a 75 mg tablet to be taken on two consecutive days each month (2CDM) in order to optimize patient adherence. This formulation has been studied in a randomized, double-blind, parallel-group, multinational trial in 1229 postmenopausal women with osteoporosis.[1]

Controversies

In January 2006 P&G and its marketing partner Sanofi-Aventis filed a Lanham Act false claims lawsuit against rival drugmakers Roche and GlaxoSmithKline claiming false advertising about Boniva.[2] The manufacturers of Boniva, a rival bisphosphonate, were accused in the suit of causing a "serious public health risk" through misrepresentation of scientific findings. In a ruling on September 7, 2006 U.S. District Judge Paul A. Crotty rejected P&G's attempted injunction. P&G was criticized for attempting to "preserve its market share by denigrating Boniva". Judge Crotty wrote that "Roche was clearly entitled to respond with its own data, provided that the data was truthfully and accurately presented".[3]

In 2006, P&G faced controversy over its handling of clinical research involving risedronate (News Reports[4] and discussion).[5]

In common with other bisphosphonate drugs, risedronate appears to be associated with the rare side effect osteonecrosis of the jaw, often preceded by dental procedures inducing trauma to the bone.

See also

References

  1. ↑ Frampton JE. Risedronate on Two Consecutive Days per Month : Drugs & Aging. Drugs&Aging 2009; 26(4):355-362. doi:10.2165/00002512-200926040-00006.
  2. ↑ "P&G Press statement". Uk.pg.com. Retrieved 2013-03-01.
  3. ↑ NY fed judge finds promotions for bone drug Boniva are fair Associated Press, 7 Sept 2006 Archived September 30, 2007, at the Wayback Machine.
  4. ↑ http://www.thejabberwock.org/wiki/index.php?title=Actonel_Case_Media_Reports
  5. ↑ "Scientific Misconduct Blog". Scientific-misconduct.blogspot.com. Retrieved 2013-03-01.

External links

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