DICYCLOMINE HYDROCHLORIDE tablet

Negara: Amerika Serikat

Bahasa: Inggris

Sumber: NLM (National Library of Medicine)

Beli Sekarang

Unduh Karakteristik produk (SPC)
21-05-2018

Bahan aktif:

DICYCLOMINE HYDROCHLORIDE (UNII: CQ903KQA31) (DICYCLOMINE - UNII:4KV4X8IF6V)

Tersedia dari:

Aidarex Pharmaceuticals LLC

Rute administrasi :

ORAL

Jenis Resep:

PRESCRIPTION DRUG

Indikasi Terapi:

Dicyclomine hydrochloride is indicated for the treatment of patients with functional bowel/irritable bowel syndrome. Dicyclomine hydrochloride is contraindicated in infants less than 6 months of age [see Use in Specific Populations (8.4)] , nursing mothers [see Use in Specific Populations (8.3)] , and in patients with: - unstable cardiovascular status in acute hemorrhage - myasthenia gravis [see Warnings and Precautions (5.4)] - glaucoma [see Adverse Reactions (6.3) and Drug Interactions  (7.1)] - obstructive uropathy [see Warnings and Precautions (5.8)] - obstructive disease of the gastrointestinal tract [see Warnings and Precautions (5.5)] - severe ulcerative colitis [see Warnings and Precautions (5.7)] - reflux esophagitis Teratogenic Effects: Pregnancy Category B Adequate and well-controlled studies have not been conducted with dicyclomine hydrochloride in pregnant women at the recommended doses of 80 to 160 mg/day. However, epidemiologic studies did not show an increased risk of structural malform

Ringkasan produk:

Dicyclomine Hydrochloride Tablets USP are supplied as follows: Dicyclomine hydrochloride Tablets 20 mg tablets: Blue, round, unscored, flat-faced, beveled-edge tablets, debossed WATSON and 795 on the periphery on one side and plain on the other side, in bottles of 100 and 1000. Store at Controlled Room Temperature 15°-30°C (59°-86°F). Dispense in a well-closed container as defined in USP/NF.

Status otorisasi:

Abbreviated New Drug Application

Karakteristik produk

                                DICYCLOMINE HYDROCHLORIDE- DICYCLOMINE HYDROCHLORIDE TABLET
AIDAREX PHARMACEUTICALS LLC
----------
HIGHLIGHTS OF PRESCRIBING INFORMATION
THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE
DICYCLOMINE HYDROCHLORIDE SAFELY AND
EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR DICYCLOMINE
HYDROCHLORIDE.
DICYCLOMINE HYDROCHLORIDE CAPSULES, FOR ORAL USE
DICYCLOMINE HYDROCHLORIDE TABLETS, FOR ORAL USE
INITIAL U.S. APPROVAL: 1950
RECENT MAJOR CHANGES
Warnings and Precautions, Peripheral and Central Nervous System (5.3)
07/2012
INDICATIONS AND USAGE
Dicyclomine hydrochloride is an antispasmodic and anticholinergic
(antimuscarinic) agent indicated for the treatment of
functional bowel/irritable bowel syndrome (1) (1)
DOSAGE AND ADMINISTRATION
Dosage for dicyclomine hydrochloride must be adjusted to individual
patient needs (2). If a dose is missed, patients should
continue the normal dosing schedule (2).
ORAL IN ADULTS (2.1):
Starting dose: 20 mg four times a day. After a week treatment with the
starting dose, the dose may be escalated to 40
mg four times a day, unless side effects limit dosage escalation
Discontinue dicyclomine hydrochloride if efficacy not achieved or side
effects require doses less than 80 mg per day
after two weeks of treatment
DOSAGE FORMS AND STRENGTHS
Dicyclomine hydrochloride capsules 10 mg (3)
Dicyclomine hydrochloride tablets 20 mg (3)
CONTRAINDICATIONS
Infants less than 6 months of age (4)
Glaucoma (4)
Nursing mothers (4)
Obstructive uropathy (4)
Unstable cardiovascular status in accute hemorrhage (4)
Obstructive disease of the gastrointestinal tract (4)
Myasthenia gravis (4)
Severe ulcerative colitis (4)
Reflux esophagitis (4)
WARNINGS AND PRECAUTIONS
Cardiovascular conditions: worsening of conditions (5.2)
Peripheral and central nervous system: heat prostration can occur with
drug use (fever and heat stroke due to
decreased sweating); drug should be discontinued and supportive
measures instituted (5.3)
Psychosis and delirium have been reported in patients sensitive to
anticholi
                                
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