Is normal saline used as a CVS transportation media?
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Home drugs have side effects.
It is a prescription medicine used for fluid and electrolyte replenishment.It is possible to use Normal Saline alone or with other medications.
There are other possible side effects of Normal Saline.Ask your doctor or pharmacy for more information.
Call your doctor if you have side effects.You can report side effects to the FDA.
There is a sterile, non-pyrogenic solution for fluid and electrolyte replenishment in single dose containers.There are no antimicrobial agents in it.The nominal pH is between 4.5 and 7.0.The composition, osmolarity, and ionic concentration are shown.
The osmolarity of 154 mOsmol/L is what the 0.45% Sodium Chloride Injection has.It contains both salt and chloride.
There is a osmolarity of 308 mOsmol/L in the 0.9% Sodium Chloride Injection, USP.It contains both sodium and chloride.
The flexible container is made with non-latex plastic materials specially designed for a wide range of parenteral drugs.The AVIVA container system is compatible with and appropriate for use in the administration of paclitaxel.The AVIVA container system can be used in the administration of drugs that are compatible with existing container systems.The solution contact materials do not contain plasticizers.
Class VI U.S. Pharmacopeia testing for plastic containers has shown that the container is suitable for use.The tests confirm the safety of the container system.The container is prefilled with air to facilitate drainage.External air does not need to be entered during administration.
The administration outlet port is the place to attach an IV set and the medication site is where supplemental medication can be added.The overwrap protects the container from the physical environment.
It is indicated for use as a primer solution in hemodialysis procedures.
As directed by a doctor.The patient's age, weight and clinical condition are some of the factors that affect dosage.
Parenteral drug products should be inspected for particulate matter and discoloration prior to administration.Unless solution is clear and seal is intact, do not administer.
Injections in plastic containers are intended for use with sterile equipment.
It is possible that Additives may be incompatible.There is no complete information available.They should not be used.
If available, consult with the pharmacist.In the opinion of the physician, it is advisable to use aseptic techniques.When Additives have been introduced, mix thoroughly.Do not store solutions that have Additives.
The code size is NDC Product Name 6E1313 500 0338 6333-03.
The exposure of pharmaceutical products to heat should be minimized.It's a good idea to avoid excessive heat.The product should be stored in a room temperature of 25C/ 77F.
Remove solution container by tearing overwrap.The plastic may be moist due to the absorption process.This doesn't affect the solution quality or safety.Gradually, the opacity will diminish.If you squeeze the inner bag firmly, you can check for minute leaks.If there are leaks, discard the solution.Follow directions if supplemental medication is desired.
The Baxter healthcare corporation is located in the USA.Product information can be found at 1-800-933-0303.
Infections at the site of injection, extravasation, and hypervolemia may occur because of the solution or technique of administration.
If there is an adverse reaction, stop the infusion, evaluate the patient, institute appropriate therapeutic countermeasures, and save the rest of the fluid for examination.
Caution must be exercised in the administration of the drug.
Studies haven't been done to see if there are additional drug/drug or food interactions with Sodium Chloride.
In patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema with sodium retention, the use of Sodium Chloride Injection, USP should be used with great care.
In patients with diminished renal function, the administration of USP may result in sodium retention.
Do not connect plastic containers with series connections.Air embolism is caused by residual air being drawn from one container before administration of the fluid from a secondary container is completed.If the air in the container is not fully evacuated before the administration, it can result in air embolism.
Air embolism is caused by the use of a vent in the open position.Flexible plastic containers should not be used withventilated IV sets.
During parenteral therapy or when the condition of the patient warrants such evaluation, changes in fluid balance, electrolyte concentrations, and acid base balance need to be monitored.
Studies have not been done to evaluate the effects of the injection on fertility.
Animal reproduction studies have not been done with the injection.It is not known if the injection of thesodiumchloride can cause fetal harm or affect the reproduction capacity of a pregnant woman.If a pregnant woman needs the injection, it should be given to her.
Studies haven't been done to evaluate the effects of the injection on labor and delivery.Caution should be exercised when administering this drug.
It is not known if this drug is in human milk.There are many drugs that can be found in human milk, so caution should be exercised when administering a drug to a woman.
There has not been adequate and well controlled trials to establish the safety and effectiveness of sodium chloride in children.Children should be aware of the warnings, precautions and adverse reactions in the label copy.
The number of subjects aged 65 and over was not included in the studies to see if they respond differently to younger subjects.The responses of elderly and younger patients have not been identified.In general, dose selection for an elderly patient should be cautious, starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic,renal, or cardiac function and of concurrent disease or drug therapy.
The risk of toxic reactions to this drug may be greater in patients with impaired renal function.Elderly patients are more likely to have decreased renal function, so care should be taken in dose selection.
It is a source of water and electrolytes.Depending on the clinical condition of the patient, it is capable of inducing diuresis.