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Solu Medrol Drug Description
SOLU - MEDROL
(methylprednisolone sodium succinate) for Injection, USP
NOT FOR USE IN NEONATES
CONTAINS BENZYL ALCOHOL
For Intravenous or Intramuscular Administration
DRUG DESCRIPTION
SOLU - MEDROL Sterile Powder is an anti - inflammatory glucocorticoid, which contains methylprednisolone sodium succinate as the active ingredient. SOLU - MEDROL is available in several strengths and packages for intravenous or intramuscular administration.
40 mg Act - O - Vial System (Single - Dose Vial) - Each mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 40 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.46
mg dibasic sodium phosphate dried; 25 mg lactose hydrous; 8.8 mg benzyl alcohol
added as preservative.
125 mg Act - O - Vial System (Single - Dose Vial) - Each 2 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 125 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.4
mg dibasic sodium phosphate dried; 17.6 mg benzyl alcohol added as preservative.
500 mg Vial - Each 8 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 500 mg methylprednisolone; inactive ingredients
include 6.4 mg monobasic sodium phosphate anhydrous; 69.6 mg dibasic sodium
phosphate dried.
500 mg Vial with Diluent - Each 8 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 70.2 mg benzyl alcohol added as preservative.
500 mg Act - O - Vial System (Single - Dose Vial) - Each 4 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 33.7 mg benzyl alcohol added as preservative.
1 gram Vial - Each 16 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 1 gram methylprednisolone; inactive ingredients
include 12.8 mg monobasic sodium phosphate anhydrous; 139.2 mg dibasic sodium
phosphate dried.
1 gram Act - O - Vial System (Single - Dose Vial) - Each 8 mL (when mixed)
contains methylprednisolone sodium succinate equivalent to 1 gram methylprednisolone;
inactive ingredients include 12.8 mg mononobasic sodium phosphate anhydrous;
139.2 mg dibasic sodium phosphate dried; 66.8 mg benzyl alcohol added as preservative.
2 gram Vial - Each 30.6 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 2 grams methylprednisolone; inactive ingredients
include 25.6 mg monobasic sodium phosphate anhydrous; 278 mg dibasic sodium
phosphate dried.
2 gram Vial with Diluent - Each 30.6 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 2 grams methylprednisolone;
inactive ingredients include 25.6 mg monobasic sodium phosphate anhydrous; 278
mg dibasic sodium phosphate dried; 273 mg benzyl alcohol added as preservative.
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, 0.50 osmolar; for the 125 mg per 2 mL, 500 mg per 8 mL and 1 gram per 16 mL solutions, 0.40 osmolar; for the 1 gram per 8 mL solution, 0.44 osmolar; for the 2 gram per 30.6 mL solutions, 0.42 osmolar. (Isotonic saline = 0.28 osmolar).
The formula for methylprednisolone sodium succinate is C26H33NaO8,
and it has a molecular weight of 496.53. Chemically it is pregna - 1,4 - diene - 3,20 - dione,21 - (3 - carboxy
l - oxopropoxy) - 11,17 - dihydroxy - 6 - methyl - , monosodium salt, (6‹,11®) - .
The structural formula is represented below:








Methylprednisolone sodium succinate, USP, is the sodium succinate ester of methylprednisolone.
It occurs as a white, or nearly white, odorless hygroscopic, amorphous solid. It is very soluble in water and in alcohol; it is insoluble in chloroform and is very slightly soluble in acetone.
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 methylprednisolone are required rapidly.
IMPORTANT - Use only the accompanying diluent or Bacteriostatic Water
For Injection with Benzyl Alcohol when reconstituting SOLU - MEDROL.
Use within 48 hours after mixing.Last reviewed on RxList: 7/21/2010




Solu Medrol Drug Description
SOLU - MEDROL
(methylprednisolone sodium succinate) for Injection, USP
NOT FOR USE IN NEONATES
CONTAINS BENZYL ALCOHOL
For Intravenous or Intramuscular Administration
DRUG DESCRIPTION
SOLU - MEDROL Sterile Powder is an anti - inflammatory glucocorticoid, which contains methylprednisolone sodium succinate as the active ingredient. SOLU - MEDROL is available in several strengths and packages for intravenous or intramuscular administration.
40 mg Act - O - Vial System (Single - Dose Vial) - Each mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 40 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.46
mg dibasic sodium phosphate dried; 25 mg lactose hydrous; 8.8 mg benzyl alcohol
added as preservative.
125 mg Act - O - Vial System (Single - Dose Vial) - Each 2 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 125 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.4
mg dibasic sodium phosphate dried; 17.6 mg benzyl alcohol added as preservative.
500 mg Vial - Each 8 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 500 mg methylprednisolone; inactive ingredients
include 6.4 mg monobasic sodium phosphate anhydrous; 69.6 mg dibasic sodium
phosphate dried.
500 mg Vial with Diluent - Each 8 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 70.2 mg benzyl alcohol added as preservative.
500 mg Act - O - Vial System (Single - Dose Vial) - Each 4 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 33.7 mg benzyl alcohol added as preservative.
1 gram Vial - Each 16 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 1 gram methylprednisolone; inactive ingredients
include 12.8 mg monobasic sodium phosphate anhydrous; 139.2 mg dibasic sodium
phosphate dried.
1 gram Act - O - Vial System (Single - Dose Vial) - Each 8 mL (when mixed)
contains methylprednisolone sodium succinate equivalent to 1 gram methylprednisolone;
inactive ingredients include 12.8 mg mononobasic sodium phosphate anhydrous;
139.2 mg dibasic sodium phosphate dried; 66.8 mg benzyl alcohol added as preservative.
2 gram Vial - Each 30.6 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 2 grams methylprednisolone; inactive ingredients
include 25.6 mg monobasic sodium phosphate anhydrous; 278 mg dibasic sodium
phosphate dried.
2 gram Vial with Diluent - Each 30.6 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 2 grams methylprednisolone;
inactive ingredients include 25.6 mg monobasic sodium phosphate anhydrous; 278
mg dibasic sodium phosphate dried; 273 mg benzyl alcohol added as preservative.
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, 0.50 osmolar; for the 125 mg per 2 mL, 500 mg per 8 mL and 1 gram per 16 mL solutions, 0.40 osmolar; for the 1 gram per 8 mL solution, 0.44 osmolar; for the 2 gram per 30.6 mL solutions, 0.42 osmolar. (Isotonic saline = 0.28 osmolar).
The formula for methylprednisolone sodium succinate is C26H33NaO8,
and it has a molecular weight of 496.53. Chemically it is pregna - 1,4 - diene - 3,20 - dione,21 - (3 - carboxy
l - oxopropoxy) - 11,17 - dihydroxy - 6 - methyl - , monosodium salt, (6‹,11®) - .
The structural formula is represented below:








Methylprednisolone sodium succinate, USP, is the sodium succinate ester of methylprednisolone.
It occurs as a white, or nearly white, odorless hygroscopic, amorphous solid. It is very soluble in water and in alcohol; it is insoluble in chloroform and is very slightly soluble in acetone.
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 methylprednisolone are required rapidly.
IMPORTANT - Use only the accompanying diluent or Bacteriostatic Water
For Injection with Benzyl Alcohol when reconstituting SOLU - MEDROL.
Use within 48 hours after mixing.Last reviewed on RxList: 7/21/2010




Solu Medrol Drug Description
SOLU - MEDROL
(methylprednisolone sodium succinate) for Injection, USP
NOT FOR USE IN NEONATES
CONTAINS BENZYL ALCOHOL
For Intravenous or Intramuscular Administration
DRUG DESCRIPTION
SOLU - MEDROL Sterile Powder is an anti - inflammatory glucocorticoid, which contains methylprednisolone sodium succinate as the active ingredient. SOLU - MEDROL is available in several strengths and packages for intravenous or intramuscular administration.
40 mg Act - O - Vial System (Single - Dose Vial) - Each mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 40 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.46
mg dibasic sodium phosphate dried; 25 mg lactose hydrous; 8.8 mg benzyl alcohol
added as preservative.
125 mg Act - O - Vial System (Single - Dose Vial) - Each 2 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 125 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.4
mg dibasic sodium phosphate dried; 17.6 mg benzyl alcohol added as preservative.
500 mg Vial - Each 8 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 500 mg methylprednisolone; inactive ingredients
include 6.4 mg monobasic sodium phosphate anhydrous; 69.6 mg dibasic sodium
phosphate dried.
500 mg Vial with Diluent - Each 8 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 70.2 mg benzyl alcohol added as preservative.
500 mg Act - O - Vial System (Single - Dose Vial) - Each 4 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 33.7 mg benzyl alcohol added as preservative.
1 gram Vial - Each 16 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 1 gram methylprednisolone; inactive ingredients
include 12.8 mg monobasic sodium phosphate anhydrous; 139.2 mg dibasic sodium
phosphate dried.
1 gram Act - O - Vial System (Single - Dose Vial) - Each 8 mL (when mixed)
contains methylprednisolone sodium succinate equivalent to 1 gram methylprednisolone;
inactive ingredients include 12.8 mg mononobasic sodium phosphate anhydrous;
139.2 mg dibasic sodium phosphate dried; 66.8 mg benzyl alcohol added as preservative.
2 gram Vial - Each 30.6 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 2 grams methylprednisolone; inactive ingredients
include 25.6 mg monobasic sodium phosphate anhydrous; 278 mg dibasic sodium
phosphate dried.
2 gram Vial with Diluent - Each 30.6 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 2 grams methylprednisolone;
inactive ingredients include 25.6 mg monobasic sodium phosphate anhydrous; 278
mg dibasic sodium phosphate dried; 273 mg benzyl alcohol added as preservative.
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, 0.50 osmolar; for the 125 mg per 2 mL, 500 mg per 8 mL and 1 gram per 16 mL solutions, 0.40 osmolar; for the 1 gram per 8 mL solution, 0.44 osmolar; for the 2 gram per 30.6 mL solutions, 0.42 osmolar. (Isotonic saline = 0.28 osmolar).
The formula for methylprednisolone sodium succinate is C26H33NaO8,
and it has a molecular weight of 496.53. Chemically it is pregna - 1,4 - diene - 3,20 - dione,21 - (3 - carboxy
l - oxopropoxy) - 11,17 - dihydroxy - 6 - methyl - , monosodium salt, (6‹,11®) - .
The structural formula is represented below:








Methylprednisolone sodium succinate, USP, is the sodium succinate ester of methylprednisolone.
It occurs as a white, or nearly white, odorless hygroscopic, amorphous solid. It is very soluble in water and in alcohol; it is insoluble in chloroform and is very slightly soluble in acetone.
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 methylprednisolone are required rapidly.
IMPORTANT - Use only the accompanying diluent or Bacteriostatic Water
For Injection with Benzyl Alcohol when reconstituting SOLU - MEDROL.
Use within 48 hours after mixing.Last reviewed on RxList: 7/21/2010




Solu Medrol Drug Description
SOLU - MEDROL
(methylprednisolone sodium succinate) for Injection, USP
NOT FOR USE IN NEONATES
CONTAINS BENZYL ALCOHOL
For Intravenous or Intramuscular Administration
DRUG DESCRIPTION
SOLU - MEDROL Sterile Powder is an anti - inflammatory glucocorticoid, which contains methylprednisolone sodium succinate as the active ingredient. SOLU - MEDROL is available in several strengths and packages for intravenous or intramuscular administration.
40 mg Act - O - Vial System (Single - Dose Vial) - Each mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 40 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.46
mg dibasic sodium phosphate dried; 25 mg lactose hydrous; 8.8 mg benzyl alcohol
added as preservative.
125 mg Act - O - Vial System (Single - Dose Vial) - Each 2 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 125 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.4
mg dibasic sodium phosphate dried; 17.6 mg benzyl alcohol added as preservative.
500 mg Vial - Each 8 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 500 mg methylprednisolone; inactive ingredients
include 6.4 mg monobasic sodium phosphate anhydrous; 69.6 mg dibasic sodium
phosphate dried.
500 mg Vial with Diluent - Each 8 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 70.2 mg benzyl alcohol added as preservative.
500 mg Act - O - Vial System (Single - Dose Vial) - Each 4 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 33.7 mg benzyl alcohol added as preservative.
1 gram Vial - Each 16 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 1 gram methylprednisolone; inactive ingredients
include 12.8 mg monobasic sodium phosphate anhydrous; 139.2 mg dibasic sodium
phosphate dried.
1 gram Act - O - Vial System (Single - Dose Vial) - Each 8 mL (when mixed)
contains methylprednisolone sodium succinate equivalent to 1 gram methylprednisolone;
inactive ingredients include 12.8 mg mononobasic sodium phosphate anhydrous;
139.2 mg dibasic sodium phosphate dried; 66.8 mg benzyl alcohol added as preservative.
2 gram Vial - Each 30.6 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 2 grams methylprednisolone; inactive ingredients
include 25.6 mg monobasic sodium phosphate anhydrous; 278 mg dibasic sodium
phosphate dried.
2 gram Vial with Diluent - Each 30.6 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 2 grams methylprednisolone;
inactive ingredients include 25.6 mg monobasic sodium phosphate anhydrous; 278
mg dibasic sodium phosphate dried; 273 mg benzyl alcohol added as preservative.
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, 0.50 osmolar; for the 125 mg per 2 mL, 500 mg per 8 mL and 1 gram per 16 mL solutions, 0.40 osmolar; for the 1 gram per 8 mL solution, 0.44 osmolar; for the 2 gram per 30.6 mL solutions, 0.42 osmolar. (Isotonic saline = 0.28 osmolar).
The formula for methylprednisolone sodium succinate is C26H33NaO8,
and it has a molecular weight of 496.53. Chemically it is pregna - 1,4 - diene - 3,20 - dione,21 - (3 - carboxy
l - oxopropoxy) - 11,17 - dihydroxy - 6 - methyl - , monosodium salt, (6‹,11®) - .
The structural formula is represented below:








Methylprednisolone sodium succinate, USP, is the sodium succinate ester of methylprednisolone.
It occurs as a white, or nearly white, odorless hygroscopic, amorphous solid. It is very soluble in water and in alcohol; it is insoluble in chloroform and is very slightly soluble in acetone.
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 methylprednisolone are required rapidly.
IMPORTANT - Use only the accompanying diluent or Bacteriostatic Water
For Injection with Benzyl Alcohol when reconstituting SOLU - MEDROL.
Use within 48 hours after mixing.Last reviewed on RxList: 7/21/2010




Solu Medrol Drug Description
SOLU - MEDROL
(methylprednisolone sodium succinate) for Injection, USP
NOT FOR USE IN NEONATES
CONTAINS BENZYL ALCOHOL
For Intravenous or Intramuscular Administration
DRUG DESCRIPTION
SOLU - MEDROL Sterile Powder is an anti - inflammatory glucocorticoid, which contains methylprednisolone sodium succinate as the active ingredient. SOLU - MEDROL is available in several strengths and packages for intravenous or intramuscular administration.
40 mg Act - O - Vial System (Single - Dose Vial) - Each mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 40 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.46
mg dibasic sodium phosphate dried; 25 mg lactose hydrous; 8.8 mg benzyl alcohol
added as preservative.
125 mg Act - O - Vial System (Single - Dose Vial) - Each 2 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 125 mg methylprednisolone;
inactive ingredients include 1.6 mg monobasic sodium phosphate anhydrous; 17.4
mg dibasic sodium phosphate dried; 17.6 mg benzyl alcohol added as preservative.
500 mg Vial - Each 8 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 500 mg methylprednisolone; inactive ingredients
include 6.4 mg monobasic sodium phosphate anhydrous; 69.6 mg dibasic sodium
phosphate dried.
500 mg Vial with Diluent - Each 8 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 70.2 mg benzyl alcohol added as preservative.
500 mg Act - O - Vial System (Single - Dose Vial) - Each 4 mL (when mixed) contains
methylprednisolone sodium succinate equivalent to 500 mg methylprednisolone;
inactive ingredients include 6.4 mg monobasic sodium phosphate anhydrous; 69.6
mg dibasic sodium phosphate dried; 33.7 mg benzyl alcohol added as preservative.
1 gram Vial - Each 16 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 1 gram methylprednisolone; inactive ingredients
include 12.8 mg monobasic sodium phosphate anhydrous; 139.2 mg dibasic sodium
phosphate dried.
1 gram Act - O - Vial System (Single - Dose Vial) - Each 8 mL (when mixed)
contains methylprednisolone sodium succinate equivalent to 1 gram methylprednisolone;
inactive ingredients include 12.8 mg mononobasic sodium phosphate anhydrous;
139.2 mg dibasic sodium phosphate dried; 66.8 mg benzyl alcohol added as preservative.
2 gram Vial - Each 30.6 mL (when mixed as directed) contains methylprednisolone
sodium succinate equivalent to 2 grams methylprednisolone; inactive ingredients
include 25.6 mg monobasic sodium phosphate anhydrous; 278 mg dibasic sodium
phosphate dried.
2 gram Vial with Diluent - Each 30.6 mL (when mixed as directed) contains
methylprednisolone sodium succinate equivalent to 2 grams methylprednisolone;
inactive ingredients include 25.6 mg monobasic sodium phosphate anhydrous; 278
mg dibasic sodium phosphate dried; 273 mg benzyl alcohol added as preservative.
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, 0.50 osmolar; for the 125 mg per 2 mL, 500 mg per 8 mL and 1 gram per 16 mL solutions, 0.40 osmolar; for the 1 gram per 8 mL solution, 0.44 osmolar; for the 2 gram per 30.6 mL solutions, 0.42 osmolar. (Isotonic saline = 0.28 osmolar).
The formula for methylprednisolone sodium succinate is C26H33NaO8,
and it has a molecular weight of 496.53. Chemically it is pregna - 1,4 - diene - 3,20 - dione,21 - (3 - carboxy
l - oxopropoxy) - 11,17 - dihydroxy - 6 - methyl - , monosodium salt, (6‹,11®) - .
The structural formula is represented below:








Methylprednisolone sodium succinate, USP, is the sodium succinate ester of methylprednisolone.
It occurs as a white, or nearly white, odorless hygroscopic, amorphous solid. It is very soluble in water and in alcohol; it is insoluble in chloroform and is very slightly soluble in acetone.
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 methylprednisolone are required rapidly.
IMPORTANT - Use only the accompanying diluent or Bacteriostatic Water
For Injection with Benzyl Alcohol when reconstituting SOLU - MEDROL.
Use within 48 hours after mixing.Last reviewed on RxList: 7/21/2010





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Other reviews about Solu Medrol on web:

Accurate, FDA approved Solu-Medrol information for healthcare professionals and patients - brought to you by Drugs.com. Solu-Medrol Official FDA information, side effects and uses.


Methylprednisolone is a synthetic glucocorticoid or corticosteroid drug. It is sold in the USA and Canada under the brand names Medrol, Solu-Medrol and Cadista. It is also ... Methylprednisolone - Wikipedia, the free encyclopedia


Learn about the prescription medication Solu Medrol (Methylprednisolone sodium succinate), drug uses, dosage, side effects, drug interactions, warnings, reviews and patient ... Solu Medrol (Methylprednisolone sodium succinate) Drug Information ...


Physician reviewed Solu-Medrol patient information - includes Solu-Medrol description, dosage and directions. Solu-Medrol (methylprednisolone) medical facts from Drugs.com


Solu-Medrol has many side effects and treatment with this drug can be stressful. Solu-Medrol is a corticosteroid given to people with multiple sclerosis (MS) to shorten relapses. Solu-Medrol Tip - Side Effects from Solu-Medrol - Multiple ...


1 SOLU-MEDROL ® methylprednisolone sodium succinate for injection, USP For Intravenous or Intramuscular Administration DESCRIPTION SOLU-MEDROL Sterile Powder contains ... SOLU-MEDROL® methylprednisolone sodium succinate for injection, USP


Solu-Medrol is a corticosteroid given to people with multiple sclerosis (MS) to shorten relapses. Learn what to expect during your Solu-Medrol treatment. Solu-Medrol Experience – Side Effects from Solu-Medrol ...


Solu-Medrol, Medrol, Duralone, Medralone, and M-Prednisol are all trade names for generic drug Methylprednisolone. Solu-Medrol has many uses in the treatment of cancer and is ... Solu-Medrol, Medrol, Methylprednisolone, Duralone - Chemotherapy ...


Find patient medical information for Solu-Medrol Inj on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings. Solu-Medrol Inj : Uses, Side Effects, Interactions, Pictures ...


SOLUMEDROL (Corticosteroid) PROTOCOL: For Neuromuscular Diseases Admission testing. History & Physical examination Blood: CBC, Electrolytes, Blood Glucose, PT, PTT Solumedrol protocol





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