Nutriflex Peri/Nutriflex Plus Adverse Reactions

Concise Prescribing Info Full Prescribing Info Contents Description Action Indications/Uses Dosage/Direction for Use Overdosage Contraindications Special Precautions Use In Pregnancy & Lactation Adverse Reactions Drug Interactions Caution For Usage Storage MIMS Class ATC Classification Regulatory Classification Presentation/Packing

Full Prescribing Info

Adverse Reactions

Summary of the safety profile: Undesirable systemic effects with the components of Nutriflex Peri/Nutriflex Plus are rare (≥ 1/10,000 to < 1/1,000) and usually related to inadequate dosage and/or infusion rate. Those that do occur are usually reversible and regress when therapy is discontinued.
Listing of undesirable effects: Undesirable effects are listed according to their frequencies as follows: Very common (≥ 1/10); Common (≥ 1/100 to < 1/10); Uncommon (≥ 1/1,000 to < 1/100); Rare (≥ 1/10,000 to < 1/1,000); Very rare (< 1/10,000); Not known (frequency cannot be estimated from the available data).
Gastrointestinal disorders: Rare: Nausea, vomiting, decreased appetite.
General disorders and administration site conditions (for Nutriflex Peri only): Common: Vein irritation, phlebitis, thrombophlebitis.
Information on particular undesirable effects: If nausea, vomiting or decreased appetite occur, the infusion should be discontinued or, if appropriate, the infusion should be continued at a lower dose level.
For Nutriflex Peri, if signs of vein wall irritation, phlebitis or thrombophlebitis occur, change of the infusion site should be considered.

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Nutriflex Peri/Nutriflex Plus Adverse Reactions

Manufacturer:

B. Braun

Distributor:

DKSH

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