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Microsoft word - chapter 13 drugs
Drugs in Rheumatology Practice
Dr. Shrikant Wagh
M. D., M. A. Sc.
Rheumatologist, Deenanath Mangeshkar Hospital,
Sancheti Institute of Orthopedics and Rehabilitation, Lupus Clinic, Pune
Wagh S. Drugs in Rheumatology Practice In Wagh S. (Ed). Rheumatology in Primary Care 1st Edition KYA Foundation 2012; pp 123-127
Various drugs are mainstay in the treatment of rheumatic diseases. There is good evidence that they modify disease severity and progression. Most of the rheumatological diseases are chronic and hence, drugs must be taken continuously unless otherwise advised. The situation is akin to diabetes, blood pressure and heart diseases. Number of drugs are initially prescribed in diseases such as rheumatoid arthritis and systemic lupus erythematosus. Some of these drugs are slowly withdrawn in 6-12 months after a satisfactory disease control is achieved. Some drugs may have to be taken for life time.
These drugs have excellent risk-benefit profile and adverse events due to drugs are well documented. Adverse events must be monitored by blood and other examinations at regular intervals. Adverse events are like road accidents. No one stops traveling on roads for fear of an accident. Drug induced adverse events are usually mild and easily treatable. Most of them can be anticipated by careful monitoring and will subside on withdrawal of offending agent. Alternate drugs for achieving disease control can then be used in such situations.
Dosages and common adverse effects of routinely prescribed disease modifying anti-rheumatic drugs (DMARDs) are given in the adjoining table (Table 1). Doses may vary according to body weight. Lower doses are advocated in children and elderly.
Table 1 Common DMARDs
acid At least 24 hrs hepatotoxicity, lung apart
hypertension, myelosuppression, hepatotoxicity
Subcutaneous injection of methotrexate is stomach-friendly and faster acting due to higher bio-availability of the drug. This is a simple and almost painless injection which patients can take themselves. The procedure is similar to insulin injection prescribed in diabetes.
Subcutaneous injection procedure:
Fill insulin syringe with prescribed dose. (Methotrexate 25 mg/ml = 40 units/ml in Insulin syringe i.e. 2.5 mg = 4 units)
Clean area over thigh or abdomen with spirit or iodine.
Pinch skin and insert needle from side parallel to skin surface.
Pull back piston. No blood should be seen in syringe.
Remove syringe and press for a while. Do not rub.
Drugs during pregnancy and lactation
Any drug should be taken in lowest possible dose and for shortest period of time (Table 2). Use short acting drugs e.g. paracetamol, ibuprofen or diclofenac for pain relief. Inadvertent exposure of drug is not an indication for termination of pregnancy. Decision regarding termination must be based on potential risk to the fetus as determined by ultrasound examination (for structural abnormalities) and amniocentesis (for chromosomal abnormalities).
Nonsteroidal anti-inflammatory drugs (NSAIDs):
Adverse effects are possible in mother as well as fetus although these drugs do not cross placenta. These drugs are categorized B in first part of pregnancy. It is advisable to stop NSAIDs after 32 weeks of gestation in view of increased risk of premature closure of ductus arteriosus. Edema, raised blood pressure and masking of infection related symptoms are possible.
Hydrocortisone, cortisone and prednisone have minimal or no effect on fetus. Betamethasone and dexamethasone cross placenta and are used for fetal abnormalities. Use lowest possible dose (prednisone < 20 mg/day). Avoid abrupt discontinuation. Common side effects include edema, infection, muscle weakness, osteoporosis, osteonecrosis and hyperglycemia. High doses can cause cleft palate (during first trimester), adrenal suppression and growth retardation in fetus. Most complications are dose related.
Table A2.2 DMARDs in Pregnancy and Lactation
around this time. Potentialbut unproven risk.
Excreted in rat milk but notin human milk.
*Check blood of baby for hematologic, hepatic and renal abnormalities at
regular intervals. Breast feeding may be stopped at an early date.
Drug categories :
No controlled studies in humans. Safe in animals. Risks observed in
animals unproven in humans. Use with caution.
Unsafe in animals. No studies in humans. Use only if benefits outweigh risks. Risk cannot be ruled out.
Evidence of risk in humans. Benefits may be acceptable with due risk.
Fetal abnormalities observed. Drug is contraindicated in pregnancy.
Sulphasalazine reduces sperm count in up to 70% patients. Sperm count returns to normal 3 months after stopping this drug. Cyclophosphamide therapy, too, reduces sperm counts in a dose and duration dependant manner. Testosterone injection appears to normalize sperm counts in such cases. A recent report of 40 men taking methotrexate at the time of conception did not appear to cause any congenital malformations.
RESENHAS CALDEIRA, Teresa P. do Rio. 2000. Ci - dade de Muros: Crime, Segregação e disjuntiva”. Este conceito, embora não Cidadania em São Paulo . São Paulo: Editora 34/Edusp. 399 pp. vro, é a mola mestra da argumentaçãoda autora. Caldeira avalia que uma dasmaiores contradições do Brasil contem- Andréa Moraes Alves processo de transição democrática, sedese
Allegato 10 PERCORSO DIAGNOSTICO-TERAPEUTICO DELLA SINDROME DI RETT PREMESSA La sindrome di Rett (RTT) è una grave patologia neurologica, che colpisce prevalentemente le femmine, con un’incidenza variabile tra 1:10000 e 1:15000. La patologia è stata descritta per la prima volta nel 1966 da parte del medico austriaco Andreas Rett, e successivamente resa nota a tutto il mondo dal