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SIVEXTRO Film-coated tablet (2020)

Αναφορές

Βιβλιογραφική αναφορά

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Περιεχόμενα

Name of the medicinal product

Sivextro 200 mg film-coated tablets.

Qualitative and quantitative composition

Each film-coated tablet contains 200 mg tedizolid phosphate. For the full list of excipients, see section 6.1.

Pharmaceutical form

Film-coated tablet (tablet). Oval (13.8 mm long by 7.4 mm wide) yellow film-coated tablet debossed with TZD on the obverse side and 200 on the reverse side.

Therapeutic indications

Sivextro is indicated for the treatment of acute bacterial skin and skin structure infections (ABSSSI) in adults and adolescents 12 years of age and older (see sections 4.4 and 5.1). Consideration should ...

Posology and method of administration

Posology Tedizolid phosphate film-coated tablets or powder for concentrate for solution for infusion may be used as initial therapy. Patients who commence treatment on the parenteral formulation may be ...

Contraindications

Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.

Special warnings and precautions for use

Patients with neutropenia The safety and efficacy of tedizolid phosphate in patients with neutropenia (neutrophil counts <1,000 cells/mm³) have not been investigated. In an animal model of infection, the ...

Interaction with other medicinal products and other forms of interaction

Pharmacokinetic interactions In a clinical study comparing the single dose (10 mg) pharmacokinetics of rosuvastatin (Breast Cancer Resistant Protein [BCRP] substrate) alone or in combination with tedizolid ...

Fertility, pregnancy and lactation

Pregnancy There are no data from the use of tedizolid phosphate in pregnant women. Studies in mice and rats showed developmental effects (see section 5.3). As a precautionary measure, it is preferable ...

Effects on ability to drive and use machines

Sivextro may have a minor influence on the ability to drive and use machines as it may cause dizziness, fatigue or, uncommonly, somnolence (see section 4.8).

Undesirable effects

Summary of the safety profile Adults The most frequently reported adverse reactions occurring in patients receiving tedizolid phosphate in the pooled controlled Phase 3 clinical studies (tedizolid phosphate ...

Overdose

In the event of overdose, Sivextro should be discontinued and general supportive treatment given. Haemodialysis does not result in meaningful removal of tedizolid from systemic circulation. The highest ...

Pharmacodynamic properties

Pharmacotherapeutic group: Antibacterials for systemic use, other antibacterials ATC code: J01XX11 Mechanism of action Tedizolid phosphate is an oxazolidinone phosphate prodrug. The antibacterial activity ...

Pharmacokinetic properties

Oral and intravenous tedizolid phosphate is a prodrug that is rapidly converted by phosphatases to tedizolid, the microbiologically active moiety. Only the pharmacokinetic profile of tedizolid is discussed ...

Preclinical safety data

Long-term carcinogenicity studies have not been conducted with tedizolid phosphate. Repeated oral and intravenous dosing of tedizolid phosphate in rats in 1-month and 3-month toxicology studies produced ...

List of excipients

Tablet core: Microcrystalline cellulose Mannitol Povidone Crospovidone Magnesium stearate Film coat: Polyvinyl alcohol Titanium dioxide (E171) Macrogol Talc Yellow iron oxide (E172)

Incompatibilities

Not applicable.

Shelf life

3 years.

Special precautions for storage

This medicinal product does not require any special storage conditions.

Nature and contents of container

6 × 1 tablets in aluminum/Polyethylene Terephthalate (PET)/Paper foil and polyvinyl chloride (PVC)/polyvinylidene chloride (PVdC) clear film perforated child-resistant unit-dose blisters.

Special precautions for disposal and other handling

No special requirements.

Marketing authorization holder

Merck Sharp & Dohme B.V., Waarderweg 39, 2031, BN Haarlem, The Netherlands

Marketing authorization number(s)

EU/1/15/991/001

Date of first authorization / renewal of the authorization

Date of first authorisation: 23 March 2015 Date of latest renewal: 09 January 2020

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