Prednisone is a corticosteroid sold in the U.S. under 5 brand and generic names, for adrenal insufficiency, autoimmune hemolytic anemia and asthma. Below: what the FDA label says, every product that contains it, what the pills look like, and its recall record.
From the FDA label for Prednisone (application ANDA085162). Other prednisone products — different forms, different strengths — are dosed differently. Follow the label for the one you were prescribed.
Gastric irritation may be reduced if taken before, during, or immediately after meals or with food or milk. The maximal activity of the adrenal cortex is between 2 am and 8 am, and it is minimal between 4 pm and midnight. Exogenous corticosteroids suppress adrenocorticoid activity the least when given at the time of maximal activity (am) for single dose administration. Therefore, it is recommended that prednisone be administered in the morning prior to 9 am and when large doses are given, administration of antacids between meals to help prevent peptic ulcers. Multiple dose therapy should be evenly distributed in evenly spaced intervals throughout the day. Dietary salt restriction may be advisable in patients. Do not stop taking this medicine without first talking to your doctor. Avoid abrupt withdraw of therapy. The initial dosage of prednisone may vary from 5 mg to 60 mg per day, depending on the specific disease entity being treated. In situations of less severity lower doses will generally suffice, while in selected patients higher initial doses may be required. The initial dosage should be maintained or adjusted until a satisfactory response is noted. If after a reasonable period of time there is a lack of satisfactory clinical response, prednisone should be discontinued and the patient transferred to other appropriate therapy. IT SHOULD BE EMPHASIZED THAT DOSAGE…
(listed alphabetically, under each subsection) The following adverse reactions have been reported with prednisone or other corticosteroids: Allergic Reactions anaphylactoid or hypersensitivity reactions, anaphylaxis, angioedema. Cardiovascular System bradycardia, cardiac arrest, cardiac arrhythmias, cardiac enlargement, circulatory collapse, congestive heart failure, ECG changes caused by potassium deficiency, edema, fat embolism, hypertension or aggravation of hypertension, hypertrophic cardiomyopathy in premature infants, myocardial rupture following recent myocardial infarction (see WARNINGS: Cardio-Renal), necrotizing angiitis, pulmonary edema, syncope, tachycardia, thromboembolism, thrombophlebitis, vasculitis. Dermatologic acne, acneiform eruptions, allergic dermatitis, alopecia, angioedema, angioneurotic edema, atrophy and thinning of skin, dry scaly skin, ecchymoses and petechiae (bruising), erythema, facial edema, hirsutism, impaired wound healing, increased sweating, Karposi’s sarcoma (see PRECAUTIONS: General Precautions), lupus erythematosus-like lesions, perineal irritation, purpura, rash, striae, subcutaneous fat atrophy, suppression of reactions to skin tests, striae, telangiectasis, thin fragile skin, thinning scalp hair, urticaria. Endocrine Adrenal insufficiency-greatest potential caused by high potency glucocorticoids with long duration of action (associated…
Same active ingredient — different manufacturer, form, price and FDA recall record. That last one is what our independent score measures.
| # | Drug | Rating | Type | Form | Generic? | Typical price | |
|---|---|---|---|---|---|---|---|
| 1 | 70/100 | Prescription | Solution | Generic | $2 | View → | |
| 2 | Not yet rated | Prescription | Tablet | Generic | $2 |
Imprint codes, colour and shape from the FDA’s labelling data. Match the imprint on your pill — or search any imprint.
| Imprint | Strength | Colour | Shape | Maker |
|---|---|---|---|---|
| 060 | 20 mg | white | round | — |
| 5094;V | 5 mg | white | round | — |
| 54;612 | 5 mg | white | round | — |
| P20 | 20 mg | white | round | — |
| DAN;DAN;5442 | 10 mg | white | round | — |
The elimination half-life of prednisone is roughly 2 to 4 hours (short). Prednisone is a prodrug: the liver completely converts it to prednisolone, its active form. The FDA prednisolone label gives prednisolone a plasma elimination half-life of 2 to 4 hours, and the FDA RAYOS (prednisone) label states the terminal half-life of prednisone itself is 2 to 3 hours — so the active metabolite is NOT materially longer. Note that this blood half-life is much shorter than the drug's anti-inflammatory/biological effect, which lasts far longer (adrenal suppression persists roughly a day or more after a dose). Prednisolone is 70 to 90 percent protein-bound and cleared by the liver, so clearance can vary with liver function.
Prednisolone Sodium Phosphate Oral Solution (FDA label, DailyMed) ↗Half-life is how long the body takes to clear half a dose. It is not the same as how long a drug test can detect it, and it varies with age, kidney and liver function.
Sources: FDA openFDA drug label, National Drug Code Directory, and Enforcement (recall) database. This page reproduces public FDA data and is not medical advice. Dosing is set by your prescriber.
Prednisone tablets are contraindicated in systemic fungal infections and known hypersensitivity to components.
| 3 | Not yet rated | Prescription | Tablet | Generic | $2 | View → |
| 4 | Not yet rated | Prescription | Tablet | Generic | $2 | View → |
| 5 | Not yet rated | Prescription | Tablet | Generic | $2 | View → |