It is recommended to breastfeed exclusively for six months and then while introducing to other food sources extend it to twelve months. In this duration most mothers will need help of some sort of medication, It could be for short term like could and flue or it could be something chronic like Arthritis or Diabetes and here comes the question of safety of medication in use. In this post we will figure out what is Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating and whether its safe to use Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating while nursing or not.
What is Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating ?
Prednisolone sodium phosphate orally disintegrating tablets are indicated in the treatment of the following diseases or conditions: Prednisolone sodium phosphate is a corticosteroid indicated •as an anti-inflammatory or immunosuppressive agent for certain allergic, dermatologic, gastrointestinal, hematologic, ophthalmologic, nervous system, renal, respiratory, rheumatologic, specific infectious diseases or conditions and organ transplantation (1) •for the treatment of certain endocrine conditions (1) •for palliation of certain neoplastic conditions (1) 1.1 Allergic Conditions Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in adult and pediatric populations with: •Atopic dermatitis •Drug hypersensitivity reactions •Seasonal or perennial allergic rhinitis •Serum sickness 1.2 Dermatologic Diseases •Bullous dermatitis herpetiformis •Contact dermatitis •Exfoliative erythroderma •Mycosis fungoides •Pemphigus •Severe erythema multiforme (Stevens-Johnson Syndrome) 1.3 Endocrine Conditions •Congenital adrenal hyperplasia •Hypercalcemia of malignancy •Nonsuppurative thyroiditis •Primary or secondary adrenocortical insufficiency: hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable. 1.4 Gastrointestinal Diseases During acute episodes in: •Crohn’s Disease •Ulcerative colitis 1.5 Hematologic Diseases •Acquired (autoimmune) hemolytic anemia •Diamond-Blackfan anemia •Idiopathic thrombocytopenic purpura in adults •Pure red cell aplasia •Secondary thrombocytopenia in adults 1.6 Neoplastic Conditions For the treatment of: •Acute leukemia •Aggressive lymphomas 1.7 Nervous System Conditions •Acute exacerbations of multiple sclerosis •Cerebral edema associated with primary or metastatic brain tumor, craniotomy or head injury 1.8 Ophthalmic Conditions •Sympathetic ophthalmia •Uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids 1.9 Conditions Related to Organ Transplantation •Acute or chronic solid organ rejection 1.10 Pulmonary Diseases •Acute exacerbations of chronic obstructive pulmonary disease (COPD) •Allergic bronchopulmonary aspergillosis •Aspiration pneumonitis •Asthma •Fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate chemotherapy •Hypersensitivity pneumonitis •Idiopathic bronchiolitis obliterans with organizing pneumonia •Idiopathic eosinophilic pneumonias •Idiopathic pulmonary fibrosis Pneumocystis carinii pneumonia (PCP) associated with hypoxemia occurring in an HIV (+) individual who is also under treatment with appropriate anti-PCP antibiotics •Symptomatic sarcoidosis 1.11 Renal Conditions To induce a diuresis or remission of proteinuria in nephrotic syndrome, without uremia, of the idiopathic type or that due to lupus erythematosus 1.12 Rheumatologic Conditions As adjunctive therapy for short term administration (to tide the patient over an acute episode or exacerbation) in: •Acute gouty arthritis During an exacerbation or as maintenance therapy in selected cases of: •Ankylosing spondylitis •Dermatomyositis/polymyositis •Polymyalgia rheumatica/temporal arteritis •Psoriatic arthritis •Relapsing polychondritis •Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low dose maintenance therapy) •Sjogren’s syndrome •Systemic lupus erythematosus •Vasculitis 1.13 Specific Infectious Diseases •Trichinosis with neurologic or myocardial involvement •Tuberculous meningitis with subarachnoid block or impending block, (used concurrently with appropriate antituberculous chemotherapy
Is using Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating safe or dangerous while breastfeeding?
As per our analysis Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating contains only one ingredient and that is Prednisolone 21-phosphate. We have analyzed Prednisolone 21-phosphate and it seems to be safe to use Prednisolone 21-phosphate while breastfeeding, that means usage of Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating shall be safe while breastfeeding. Below you can check more details of Prednisolone 21-phosphate usage in breastfeeding. We recommend you to go through provided detailed analysis as below take decision accordingly.
Statement of Manufacturer/Labeler about breastfeeding usage
8.3 Nursing Mothers Prednisolone is secreted in human milk. Reports suggest that prednisolone concentrations in human milk are 5% to 25% of maternal serum levels, and that total infant daily doses are small, about 0.14% of the maternal daily dose. Therefore, caution should be exercised when prednisolone is administered to a nursing woman. High doses of corticosteroids for long periods could potentially produce problems in infant growth and development and interfere with endogenous corticosteroid production. The risk of infant exposure to prednisolone through breast milk should be weighed against the known benefits of breast-feeding for both the mother and baby. If prednisolone must be prescribed to a breast-feeding mother, the lowest dose should be prescribed to achieve the desired clinical effect.
Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating Breastfeeding Analsys
SafeCAS Number: 50-24-8
Excreted into breast milk in non-significant amount with no problems reported in breastfed infants whose mothers were treated at a daily dose as high as 7.5 mg for a long time period. At a daily dose of 60 mg used for treatment of Herpes or Gestational Pemphigus no harm effects on breastfed infants have been reported. On long term treatments it would be advisable to wait for 3 - 4 hours until the next nurse to minimize the transfer of drug to breast milk. At high doses, intra-articular treatment with other steroid drugs (Triamcinolone) have transiently affected milk production. Steroids administered before delivery may delay initiation of phase II of Lactogenesis ("milk come in") and decrease milk production in the first postpartum week. Decreased production has been seen while taking Dexametasone. Steroid drugs are commonly used for Pediatric treatment with no side effects when infrequently used and for short-time periods. The American Academy of Pediatrics rates it compatible with breastfeeding. WHO Model List of Essential Medicines (2002) rates it compatible with breastfeeding
Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating Breastfeeding Analsys - 2
CAS Number: 50-24-8

Amounts of prednisolone in breastmilk are very low. No adverse effect have been reported in breastfed infants with maternal use of any corticosteroid during breastfeeding. With high maternal doses, avoiding breastfeeding for 4 hours after a dose should markedly decrease the dose received by the infant. However, this maneuver is not necessary with short-term use. High doses might occasionally cause temporary loss of milk supply. Because absorption from the eye is limited, ophthalmic prednisolone would not be expected to cause any adverse effects in breastfed infants. To substantially diminish the amount of drug that reaches the breastmilk after using eye drops, place pressure over the tear duct by the corner of the eye for 1 minute or more, then remove the excess solution with an absorbent tissue.

What if I already have used Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating?
It is always a good idea to keep your healthcare provider or doctor informed about your drug usage during pregnancy and breastfeeding but if you have not informed your doctor about Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating and have used it then do not panic as Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating is mostly safe in breastfeeding and should not cause any harm to your baby.
My doctor has prescribed me Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating, what should I do?
Usage of Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating is safe for nursing mothers and baby, No worries.
If I am using Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating, will my baby need extra monitoring?
No
Who can I talk to if I have questions about usage of Prednisolone Sodium Phosphate | Prednisolone Tablet, Orally Disintegrating in breastfeeding?
US
National Womens Health and Breastfeeding Helpline: 800-994-9662 (TDD 888-220-5446) 9 a.m. and 6 p.m. ET, Monday through Friday
UK
National Breastfeeding Helpline: 0300-100-0212 9.30am to 9.30pm, daily
Association of Breastfeeding Mothers: 0300-330-5453
La Leche League: 0345-120-2918
The Breastfeeding Network supporter line in Bengali and Sylheti: 0300-456-2421
National Childbirth Trust (NCT): 0300-330-0700
Australia
National Breastfeeding Helpline: 1800-686-268 24 hours a day, 7 days a week
Canada
Telehealth Ontario for breastfeeding: 1-866-797-0000 24 hours a day, 7 days a week
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