The chemical name for Methylprednisolone Sodium Succinate is Reconstituted Methylprednisolone Sodium Succinate sterile powder contains benzyl alcohol, which is potentially toxic when administered locally to neural tissue
Use only the accompanying diluent or Bacteriostatic Water For Injection with Benzyl Alcohol when reconstituting SOLU-MEDROL (see DESCRIPTION )
5, 125, or 65
High dose: 30 mg/kg over 30 minutes (may repeat q4-6h) in a 48hr period
Methylprednisolone sodium succinate is soluble in water; it may be administered in a small volume of diluent and is well suited for intravenous use in situations where high blood levels of The test samples were prepared by reconstituting the methylprednisolone sodium succinate, adding the required amount of drug to the AutoDose Infusion System bags, and diluting to the target concentrations of 100 mg/100 mL and 1 gram/100 mL with 0
Methylprednisolone sodium succinate, USP, occurs as a white, or nearly white, odorless hygroscopic, amorphous solid
The structural formula is represented below: Methylprednisolone Sodium Succinate, USP is soluble in water; it may be administered PMID: 23981837 Abstract The chemical stability of methylprednisolone sodium succinate (10 mg/mL) in 0
Exposure to excessive amounts of benzyl alcohol has been associated with toxicity (hypotension, metabolic acidosis), particularly in neonates, and an increased incidence of kernicterus The nurse is reconstituting methylprednisolone sodium succinate for IM injection Place appropriately prepare the medication All options must be used
5, very soluble in water and in alcohol, slightly soluble in acetone and practically insoluble in chloroform and ether
IMPORTANT - Use only Water for Injection or Bacteriostatic Water for Injection with Benzyl Alcohol when reconstituting methylprednisolone sodium succinate for injection Methylprednisolone Sodium Succinate is the sodium succinate ester of methylprednisolone, and it occurs as a white, or nearly white, odorless hygroscopic, amorphous solid
Use within 48 hours after mixing
Decreased effectiveness of concomitant vaccines, interacts with skin tests
1
Mycamine (micafungin sodium) [Package Insert]
Fingerstick blood glucose measurements are prescribed before meals and at bedtime with regular insulin based on a sliding scale
Store reconstituted solution (not further diluted) at controlled room HOW SUPPLIED
For Intravenous or Intramuscular Administration DESCRIPTION Methylprednisolone Sodium Succinate for Injection, USP, Sterile Powder is an anti‑inflammatory glucocorticoid, which contains Methylprednisolone SOLU-MEDROL- methylprednisolone sodium succinate injection, When necessary, the pH of each formula was adjusted with sodium hydroxide so that the pH of the reconstituted solution is within the USP specified range of 7 to 8 and the tonicities are, for the 40 mg per mL solution, 0
When necessary, the pH of each formula was adjusted with sodium hydroxide so that the pH of the reconstituted solution is within the USP specified range of 7 to 8
IMPORTANT — Use only Water for Injection USP or Bacteriostatic Water for Injection USP with Benzyl Alcohol when reconstituting Methylprednisolone P
Succinate Glucocorticoid
The medication may be administered in dilute solutions by admixing the reconstituted product with Dextrose 5% in Water, 0
2
) Lyophilized in container 1 Reconstituted BRAND NAME methylprednisolone sodium succinate for injection, USP For Intramuscular or intravenous uso 1 gram* Recommended Diluent Contains Benzyl Alcohol as a Preservative A) Sterile Water B Bacteriostatic Water 0
This medicine is to be given only by or under the direct supervision of your doctor
From a microbiological point of view, unless the method of opening/reconstitution/dilution precludes the risk of microbial contamination, the product should be used immediately
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Use within 48 hours after IMPORTANT - Use only Bacteriostatic Water for Injection with Benzyl Alcohol when reconstituting Methylprednisolone Sodium Succinate for Injection, USP
Use only Bacteriostatic Water For Injection with Benzyl Alcohol when reconstituting Methylprednisolone Sodium Succinate for Injection, USP (see DESCRIPTION)
326 mg equivalent to 1
Injection, methylprednisolone sodium succinate, up to 125 mg
When high dose therapy is desired, the recommended dose of SOLU-MEDROL Sterile Powder is 30 mg/kg administered intravenously over at least 30 minutes
Not for use in neonates
Methylprednisolone Solution
Use only the accompanying diluent or Bacteriostatic Water For Injection with Benzyl Alcohol when reconstituting SOLU-MEDROL (see DESCRIPTION )
for reconstituting Methylprednisolone Sodium Succinate for Injection products contains benzyl alcohol
Nausea, vomiting, heartburn, headache, dizziness, trouble sleeping, appetite changes, increased sweating, acne, or pain/redness/swelling at the injection site may occur
After reconstituting as directed, contains benzyl alcohol
Methylprednisolone sodium succinate, USP, is the sodium succinate ester of methylprednisolone, and it occurs as a white, or nearly white, odorless
9% sodium chloride injection has been studied at 25 deg C and 5 deg C
IMPORTANT - Use only Bacteriostatic Water For Injection with Benzyl Alcohol when reconstituting Reconstituted Methylprednisolone Sodium Succinate sterile powder contains benzyl alcohol, which is potentially toxic when administered locally to neural tissue
01 mmoL Na
MethylPREDNIsolone sodium succinate SWFI, NS Manufacturer PI recommends reconstitution in SWFI
Study with Quizlet and memorize flashcards containing terms like A client with type 1 diabetes has a prescription for 30 units of insulin glargine at bedtime
How to use Solu-Medrol Solution, Reconstituted (Recon Soln) Methylprednisolone sodium succinate, USP, is the sodium succinate ester of methylprednisolone, and it occurs as a white, or nearly white, odorless hygroscopic, amorphous solid
3 Pediatrics Methylprednisolone Sodium Succinate for Injection Page 9 of 42 Compatibility The compatibility and stability of Methylprednisolone Sodium Succinate for Injection in Store unreconstituted product at controlled room temperature 20° to 25°C (68° to 77°F) [see USP]
2 mg dibasic sodium phos-phate dried; and benzyl alcohol
The test samples were prepared by reconstituting the methylprednisolone sodium succinate, adding the required amount of drug to the AutoDose Infusion System bags, and diluting to the target concentrations of 100 mg/100 mL and 1 gram/100 mL with 0
Methylprednisolone sodium succinate for injection, USP is an anti-inflammatory glucocorticoid, which contains methylprednisolone sodium succinate as the active ingredient
Methylprednisolone succinate (Methylprednisolone hydrogen succinate) sodium, a glucocorticoid, is a immunosuppressive agent with anti-inflammatory effects
Succinate Glucocorticoid
The medication may be administered in dilute solutions by admixing the reconstituted product with Dextrose 5% in Water, 0
2
) Lyophilized in container 1 Reconstituted BRAND NAME methylprednisolone sodium succinate for injection, USP For Intramuscular or intravenous uso 1 gram* Recommended Diluent Contains Benzyl Alcohol as a Preservative A) Sterile Water B Bacteriostatic Water 0
Methylprednisolone Sodium Succinate for Injection sterile powder is contraindicated: in systemic fungal infections and patients with known hypersensitivity to the product and its constituents