Klaricid IV mg (PL /, Abbott Laboratories Ltd). No new or unexpected safety concerns arose from this application and it was therefore judged that. Indications, side effects, contraindications and other prescribing information for Klaricid IV on MIMS. Clarithromycin is indicated in: Lower respiratory tract infection: acute and chronic bronchitis and pneumonia;; Upper respiratory tract infection: sinusitis and.
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It is used to treat infections such as: In the event of severe acute hypersensitivity reactions, such as anaphylaxis, severe cutaneous adverse reactions SCAR e. Pregnancy and breast-feeding If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist before receiving the medicine as the safety of clarithromycin in pregnancy or breast-feeding is not known.
KLARICID IV 500 MG
How to klariicd Klaricid IV Keep out of the sight and reach of children Do not use after the expiry date on the carton and vial. Clarithromycin is not recommended for pregnant women.
When clarithromycin and digoxin are administered together, inhibition of Pgp by clarithromycin may lead to increased exposure to digoxin. There is a risk of serious haemorrhage and significant elevations in International Normalized Ratio INR and prothrombin time when clarithromycin is co-administered kladicid warfarin see section 4.
Klaricid Iv Injection contains Clarithromycin as an active ingredient. To view the changes to a medicine you must sign up and log in. General disorders and administration site conditions. Based on variable results obtained from studies in mice, rats, rabbits and monkeys, the possibility of adverse effects on embryofoetal development cannot be excluded. Patients receiving terfenadine who have pre-existing cardiac abnormalities or electrolyte disturbances.
Reports of rhabdomyolysis have been received for patients taking clarithromycin concomitantly with these statins. Detailed information related to Klaricid Iv Injection’s uses, composition, dosage, side effects and reviews is listed below. The use of the following drugs is strictly contraindicated due to the potential for severe drug interaction effects: The usual dose of Clarithromycin is mg three times daily for 14 days.
Acute generalised exanthematous pustulosis AGEP ,Stevens-Johnson syndrome, toxic epidermal necrolysis, drug rash with eosinophilia and systemic symptoms DRESSacne Musculoskeletal and connective tissue disorders Muscle spasms 3musculoskeletal stiffness 1myalgia 2 Rhabdomyolysis 2,6myopathy Renal and urinary disorders Blood creatinine increased 1blood urea increased 1 Renal failure, nephritis interstitial General disorders and administration site conditions Injection site phlebitis 1 Injection site pain 1injection site inflammation 1 Malaise 4pyrexia 3asthenia, chest pain 4chills 4fatigue 4 Investigations Albumin globulin ratio abnormal 1blood alkaline phosphatase increased 4blood lactate dehydrogenase increased 4 International normalised ratio increased, prothrombin time prolonged, urine colour abnormal.
This includes any possible side effects not listed in the leaflet. Hypersensitive to Clarithromycin, Erythromycin or any of the macrolide antibiotics.
Concomitant use of clarithromycin with lovastatin or simvastatin is contraindicated see 4. Please note that this medicine may be available in various strengths for each active ingredient listed above.
Macrolide-susceptible Bacteriodes fragilis; Clostridium perfringens; Peptococcus species; Peptostreptococcus species; Propionibacterium acnes.
Malaise 4pyrexia 3asthenia, chest pain 4chills 4fatigue 4. Since the microbiological activities of clarithromycin and OH-clarithromycin are different for different bacteria, the intended therapeutic effect could be impaired during concomitant administration of clarithromycin and enzyme inducers.
Post-marketing reports indicate that co-administration of clarithromycin with ergotamine or dihydroergotamine has been associated with acute ergot toxicity characterized by vasospasm, and ischaemia of the extremities and other tissues including the central nervous system. There are no data on the effect of clarithromycin on the ability to drive or use machines.
Attention should also be paid to the possibility of cross resistance between clarithromycin and other macrolide drugs, as well as lincomycin and clindamycin. If intravenous midazolam is co-administered with clarithromycin, the patient must be closely monitored to allow dose adjustment. Clarithromycin may be used in neonates and children in appropriate doses.
The recommended dose of Klaricid IV for adults and children over 12 years is 1. In the case of overdosage, Klaricid IV should be discontinued and all other appropriate supportive measures should be instituted. Burping ; dry mouth ; muscle complaints ; oral disorders ; thrombocytosis ; tremor. With intravenous use in children.
Klaricid Adult – Uses, Indications, Adverse Events
However, for patients with renal impairment, the following dosage adjustments should be considered: Store in the original container. Injection site pain 1injection site inflammation 1.
To bookmark a medicine you must sign up and log in. What precautions should you take while using Klaricid Iv Injection? Company contact details Mylan Products Limited. You may need to read klaricif again.