RIFAMPIN capsule

国: アメリカ合衆国

言語: 英語

ソース: NLM (National Library of Medicine)

有効成分:

RIFAMPIN (UNII: VJT6J7R4TR) (RIFAMPIN - UNII:VJT6J7R4TR)

から入手可能:

REMEDYREPACK INC.

INN（国際名）:

RIFAMPIN

構図:

RIFAMPIN 300 mg

投与経路:

ORAL

処方タイプ:

PRESCRIPTION DRUG

適応症:

In the treatment of both tuberculosis and the meningococcal carrier state, the small number of resistant cells present within large populations of susceptible cells can rapidly become the predominant type. Bacteriologic cultures should be obtained before the start of therapy to confirm the susceptibility of the organism to rifampin and they should be repeated throughout therapy to monitor the response to treatment. Since resistance can emerge rapidly, susceptibility tests should be performed in the event of persistent positive cultures during the course of treatment. If test results show resistance to rifampin and the patient is not responding to therapy, the drug regimen should be modified. Rifampin is indicated in the treatment of all forms of tuberculosis. A three-drug regimen consisting of rifampin, isoniazid, and pyrazinamide [e.g., RIFATER ® ] 1 is recommended in the initial phase of short-course therapy which is usually continued for 2 months. The Advisory Council for the E

製品概要:

Rifampin Capsules, USP, 150 mg opaque orange capsules printed in white on one half of the capsule in radial print “Rifampin 150” and on the other half in radial print “VP/015” Rifampin Capsules, USP, 300 mg opaque orange capsules printed in white on one half of the capsule in radial print “Rifampin 300” and on the other half in radial print “VP/018” Storage: Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F). [See USP Controlled Room Temperature]. Keep tightly closed. Store in a dry place. Avoid excessive heat.

認証ステータス:

Abbreviated New Drug Application

製品の特徴

RIFAMPIN- RIFAMPIN CAPSULE
REMEDYREPACK INC.
----------
RIFAMPIN CAPSULES, USP
RX ONLY
REV. 11/18
To reduce the development of drug-resistant bacteria and maintain the
effectiveness of rifampin
capsules USP and other antibacterial drugs, rifampin should be used
only to treat or prevent infections
that are proven or strongly suspected to be caused by bacteria.
DESCRIPTION
Rifampin capsules, USP for oral administration contain 150 mg or 300
mg rifampin per capsule. The
150 mg and 300 mg capsules also contain, as inactive ingredients:
colloidal silicon dioxide, corn starch,
FD&C Blue No. 1, FD&C Red No. 40, gelatin, lactose monohydrate,
magnesium stearate, sodium lauryl
sulfate, talc, and titanium dioxide.
The printing ink contains ammonium hydroxide, isopropyl alcohol,
n-butyl alcohol, pharmaceutical
glaze, propylene glycol, simethicone, and titanium dioxide
Rifampin is a semisynthetic antibiotic derivative of rifamycin SV.
Rifampin is a red-brown crystalline
powder very slightly soluble in water at neutral pH, freely soluble in
chloroform, soluble in ethyl
acetate and in methanol. Its molecular weight is 822.95 and its
chemical formula is C
H
N
O
.
The chemical name for rifampin is either:
3-[[(4-Methyl-1-piperazinyl)imino]methyl]rifamycin
or
5,6,9,17,19,21-hexahydroxy-23-methoxy-2,4,12,16,20,22-heptamethyl-8-[N-(4-methyl-1-
piperazinyl)formimidoyl]-2,7-(epoxypentadeca[1,11,13]trienimino)naphtho[2,1-
_b_]furan-1,11(2H)-dione
21-acetate.
Its structural formula is:
CLINICAL PHARMACOLOGY
ORAL ADMINISTRATION
Rifampin is readily absorbed from the gastrointestinal tract. Peak
serum concentrations in healthy adults
and pediatric populations vary widely from individual to individual.
Following a single 600 mg oral
dose of rifampin in healthy adults, the peak serum concentration
averages 7 mcg/mL but may vary from 4
to 32 mcg/mL. Absorption of rifampin is reduced by about 30% when the
drug is ingested with food.
43
58
4
12
Rifampin is widely distributed throughout the body. It is present in
effective concentrations in many