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- Model: 181897
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Description
Rodinir capsules are shown for treatment of infections easy and moderate severity, caused by sensitive microorganisms.
Community-acquired pneumonia caused:
- Haemophilus influenzae (including the strains producing beta lactamazu);
- Haemophilus parainfluenzae (including the strains producing beta lactamazu);
- Streptococcus pneumonia (only the strains sensitive to penicillin);
- Moraxella catarrhalis (including the strains producing beta lactamazu).
Exacerbation of chronic bronchitis, is caused:
- Haemophilus influenzae (including the strains producing beta lactamazu);
- Haemophilus parainfluenzae (including the strains producing beta lactamazu);
- Streptococcus pneumonia (only the strains sensitive to penicillin);
- Moraxella catarrhalis (including the strains producing beta lactamazu).
Acute sinusitis caused:
- Haemophilus influenzae (including the strains producing beta lactamazu);
- Streptococcus pneumonia (only the strains sensitive to penicillin);
- Moraxella catarrhalis (including the strains producing beta lactamazu).
Pharyngitis/tonsillitis caused: Streptococcus pyogenes.
Uncomplicated infections of skin and soft tissues caused:
- Staphylococcus aureus (including the strains producing beta lactamazu);
- Streptococcus pyogenes.
Structure
Active ingredient: cefdinir;
1 solid capsule contains a tsefdinira of 300 mg;
Excipients: calcium of a karmelloz, polyoxide 40 stearate, silicon dioxide colloidal, magnesium stearate solid gelatin capsule: ferrous oxide black (E172), titan dioxide (E 171), gelatin.
Contraindication
Hypersensitivity to a tsefdinir, other cephalosporins and other components of drug.
Route of administration Medicine is intended toby
for oral administration. Capsules can be accepted irrespective of meal.
Pregnant
not to apply
Feature of use
during pregnancy and feeding by a breast. ChildrenMedicine to apply
to children aged from 13 years. Drivers
does not influence.
Overdose
is not presentData on overdose of a tsefdinir at the person.
Side effects
it is frequent - diarrhea, vaginal candidiasis, nausea, a headache, an abdominal pain, a vaginitis.
Infrequently - rash, dyspepsia, a meteorism, vomiting, changes in excrements, anorexia, a constipation, dizziness, dryness in a mouth, an asthenia, insomnia, a leukorrhea, candidiasis, an itching, drowsiness.
InteractionSimultaneous use with antacids reduces
With max and extent of absorption of a tsefdinir approximately for 40%. Achievement time With max also lasts for 1 hour. At simultaneous use of these means tsefdinir it is necessary to accept at least in 2 hours prior to or in 2 hours after reception of antacids. to
It was reported about cases of a reddish color of a chair at the patients accepting tsefdinir. In many cases the patients applied at the same time ferriferous products. Red coloring can be connected with education in a digestive tract of a complex of a tsefdinir or products of its decomposition and iron, is not soaked up.
Storage conditionsto Store
at a temperature not above 25 °C out of children's reach.
Expiration date - 3 years.
Specifications
Characteristics | |
Active ingredients | Tsefdinir |
Amount of active ingredient | 300 mg |
Applicant | Rotafarm |
Code of automatic telephone exchange | J01DD15 Tsefdinir |
Interaction with food | It doesn't matter |
Light sensitivity | Not sensitive |
Market status | The branded generic |
Origin | Chemical |
Prescription status | According to the prescription |
Primary packing | blister |
Producer | SAN PHARMAVISION. A.SH. VE TIDZH |
Quantity in packing | 10 capsules |
Release form | capsules for internal use |
Route of administration | Oral |
Sign | Import |
Storage temperature | from 5 °C to 25 °C |
Trade name | Rodinir |