MethylPREDNISolone Dose Pack Side Effects
Nplate with Reconstitution Pack - Summary of Product Characteristics (SPC) - (eMC)
This document contains side effect information about methylprednisolone. Although not all of these side effects may occur, if they do occur they may need medical attention. Check with your doctor immediately if any of the following side effects occur while taking methylprednisolone:.
Some side effects of methylprednisolone may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.
Check with your health care professional if any of the following side effects continue or are bothersome or if you Thrombophlebitis Pack any questions about them:. For Healthcare Professionals Applies to methylprednisolone: The most commonly occurring side effects have included fluid retention, alteration in glucose tolerance, increased blood pressure, behavioral and mood changes, increased appetite, and weight gain; the incidence generally correlates Thrombophlebitis Pack dosage, timing of administration, and duration of treatment.
Allergic or hypersensitivity reactions; anaphylactoid Thrombophlebitis Pack, anaphylaxis, angioedema [ Ref ]. Bradycardia, cardiac arrest, cardiac arrhythmias, cardiac enlargement, circulatory collapse, congestive heart failure, fat embolism, hypertension, hypertrophic cardiomyopathy in premature infants, myocardial rupture following recent myocardial infarction, syncope, tachycardia, thromboembolism, thrombophlebitis, vasculitis, edema, hypotension [ Ref ], Thrombophlebitis Pack.
Cushingoid state, hirsutism, secondary adrenocortical and pituitary unresponsiveness particularly in times of stress, as in trauma, surgery, or illnessmoon face [ Ref ]. Abdominal Thrombophlebitis Pack, nausea, pancreatitis, peptic ulcer, perforation of the small and large intestine, ulcerative esophagitis, gastric hemorrhage, vomiting, abdominal pain, diarrhea, dyspepsia, nausea [ Ref ].
Hepatomegaly, elevation in liver enzymes, toxic hepatitis [ Ref ]. These changes have generally been small and not associated with any clinical syndrome. Toxic hepatitis has been reported with high doses of cyclically pulsed IV therapy, Thrombophlebitis Pack has been several weeks or longer. Resolution has been reported with discontinuation; however, recurrence has been reported with rechallenge.
Decreased carbohydrate and glucose tolerance, manifestations of latent diabetes, hypokalemic alkalosis, potassium loss, sodium retention, increased appetite, negative nitrogen balance due to protein catabolism, weight gain, metabolic acidosis, dyslipidemia, lipomatosis [ Ref Thrombophlebitis, ob gefährlich. Suppression of growth in pediatric patients, aseptic necrosis of femoral and humeral heads, calcinosis, Charcot-like atrophy, loss of muscle mass, muscle weakness, osteoporosis, pathologic fracture of long bones, postinjection flare, steroid myopathy, tendon rupture, particularly of the Achilles tendon, vertebral compression fractures, myalgia, muscle atrophy, osteonecrosis, neuropathic arthralgia, Thrombophlebitis Pack, growth retardation [ Ref ].
Leucocytosis [ Ref ]. Thrombophlebitis Pack infection [ Ref ]. Blindness has been reported with corticosteroid injection to scalp, tonsillar fauces, sphenopalatine ganglion. Exophthalmos, glaucoma, increased intraocular pressure, posterior subcapsular cataracts, blindness, chorioretinopathy [ Ref ].
Depression, emotional instability, euphoria, insomnia, mood swings, personality changes, psychic disorders, confusional states, Thrombophlebitis Pack, anxiety, abnormal behavior, irritability [ Ref ].
Acne, allergic dermatitis, cutaneous and subcutaneous atrophy, dry scaly skin, ecchymosis, petechiae, erythema, hyperpigmentation, hypopigmentation, impaired wound healing, increased sweating, rash, sterile abscess, striae, suppressed reactions to skin tests, thin fragile skin, thinning scalp hair, urticaria, hypertrichosis, angioedema, skin atrophy, hyperhidrosis, Thrombophlebitis Pack, pruritus [ Ref ].
Injection site infections, Thrombophlebitis Pack, injection site reactions [ Ref ]. Convulsions, headache, increased intracranial pressure with papilledema pseudotumor cerebri Thrombophlebitis Pack following discontinuation of treatment, neuritis, Thrombophlebitis Pack, neuropathy, Thrombophlebitis Pack, amnesia, dizziness [ Ref ]. Vertigo, abnormal fat deposits, malaise, sterile abscess, impaired healing, fatigue [ Ref ]. Kaposi's sarcoma [ Ref ]. Pulmonary edema, pulmonary embolism, hiccups [ Ref ].
Menstrual irregularities, increased or decreased motility and number of spermatozoa, increased urine calcium, glycosuria [ Ref ]. Thrombophlebitis Pack consult your doctor or healthcare specialist for medical advice.
You may also report side effects to the FDA. Every effort has been made to ensure that the information provided is accurate, up-to-date and complete, but no guarantee is CHI Behandlung von Krampfadern to that effect.
In addition, the drug information contained herein may Thrombophlebitis Pack time sensitive and should not be utilized as a reference resource beyond the date hereof. This material does not endorse drugs, diagnose patients, or recommend therapy. This information is a reference resource designed as supplement to, and not a substitute for, the expertise, skillknowledge, and judgement of healthcare practitioners in patient care.
The absence of a warning for a given drug or combination thereof in no way should be construed to indicate safety, effectiveness, or appropriateness for any given patient. The information contained herein is not intended to Thrombophlebitis Pack all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects.
If you have questions about the substances you are taking, Thrombophlebitis Pack, check with your doctor, nurse, or pharmacist. Inflammatory Conditions prednisonehydrocortisoneprednisolonedexamethasoneMedrolmethylprednisoloneMore Allergic Rhinitis prednisoneZyrtecpromethazinefluticasone nasalloratadineFlonaseMore Asthma prednisonetriamcinolonemontelukastSingulairipratropiumBreo ElliptaMore Osteoarthritis prednisonenaproxenCymbaltaaspirinmeloxicamibuprofenMore The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records.
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Patients should be counseled that oral contraceptives do not protect against transmission of HIV AIDS and other sexually transmitted diseases STDs such as chlamydia, genital herpes, genital warts, gonorrhea, hepatitis B, and syphilis.
The inactive ingredients present are cellulose, hypromellose, iron oxide, lactose Thrombophlebitis Pack, magnesium stearate, polacrilin potassium, polyethylene glycol, titanium dioxide, and montanic ester wax. Get emergency medical help if you have any of these signs of an allergic reaction: Stop using birth control pills and call your doctor at once if you have a serious side effect Varizen jugendliche Behandlung as:.
ALESSE levonorgestrel and ethinyl estradiol is indicated for the prevention of pregnancy in women who elect to use oral contraceptives as a method of contraception. Oral contraceptives are highly effective. Table II lists the typical accidental pregnancy rates for users of combination oral contraceptives and other methods of contraception.
Correct and consistent use of methods can result in lower failure rates. The FDA has concluded that certain combined oral contraceptives containing ethinyl estradiol and norgestrel or levonorgestrel are safe and effective for use as postcoital emergency contraception. LAM is a highly effective, temporary method of contraception.
Among typical couples who initiate use of a method not necessarily for Thrombophlebitis Pack first timethe percentage who experience an accidental pregnancy during the first year if they do not stop use for any other reason. Among couples who initiate use of a method not necessarily for the first time and who use it perfectly both consistently and correctlyThrombophlebitis Pack, the percentage who experience an accidental pregnancy during the first year if they do not stop use for any other reason, Thrombophlebitis Pack.
Among couples attempting to avoid pregnancy, the percentage who continue to use a method for one year, Thrombophlebitis Pack. The percents becoming pregnant in columns 2 and 3 are based on data from populations where contraception is not used and from women who cease using contraception in order to become pregnant. Foams, creams, Thrombophlebitis Pack, gels, vaginal suppositories, and vaginal film.
Cervical mucus ovulation method supplemented by calendar in Thrombophlebitis Pack pre-ovulatory and basal body temperature Thrombophlebitis Pack the post-ovulatory phases. With spermicidal cream or jelly. The treatment schedule is one dose within 72 hours after unprotected intercourse, and a second dose 12 hours after the first dose.
The FDA has declared the following dosage regimens of oral contraceptives to be safe and effective for emergency contraception: However, to maintain effective protection against pregnancy, another method of contraception must be used as soon as menstruation resumes, the frequency or duration of breastfeeds is reduced, Thrombophlebitis Pack, bottle feeds are introduced, or the baby reaches 6 months of age. In a clinical trial with ALESSE levonorgestrel and ethinyl estradiol tablets1, subjects had 7, cycles of use and a total of 5 pregnancies were reported.
This represents an overall pregnancy rate of 0. This rate includes patients who did not take the drug correctly. One or more pills were missed during 1, The dosage of ALESSE levonorgestrel and ethinyl estradiol is one pink tablet daily for 21 consecutive days, followed by one lightgreen inert tablet daily for 7 consecutive days, according to the Thrombophlebitis Pack schedule.
The dispenser should be kept in the wallet supplied to avoid possible fading of the pills. If the pills fade, patients should continue to take them as directed. The possibility of ovulation and conception prior to initiation of medication should be considered. The patient is instructed to begin taking ALESSE levonorgestrel and ethinyl estradiol on the first Sunday after the onset of menstruation.
If menstruation begins on a Sunday, Thrombophlebitis Pack, the first Thrombophlebitis Pack pink is taken that day. One pink tablet should be taken daily for 21 consecutive days, followed by one light-green inert tablet daily for 7 consecutive days. Withdrawal bleeding should usually occur within 3 days following discontinuation of pink tablets and may not have finished before the next pack is started.
During the first cycle, contraceptive reliance should not be placed on ALESSE levonorgestrel and ethinyl estradiol until a pink tablet has been taken daily for 7 consecutive days, and a nonhormonal back-up method of birth control should be used during those 7 days.
During the first cycle of medication, Thrombophlebitis Pack, the patient is instructed to begin taking ALESSE levonorgestrel and ethinyl estradiol during the first 24 hours of her period day one of her menstrual cycle.
If medication is begun on day one of the Thrombophlebitis Pack cycle, Thrombophlebitis Pack, no back-up contraception is necessary, Thrombophlebitis Pack. If ALESSE levonorgestrel and ethinyl estradiol tablets are started later than day one of the first menstrual cycle or postpartumcontraceptive reliance should not be placed on ALESSE levonorgestrel and ethinyl estradiol tablets until after the first 7 consecutive days of administration, Thrombophlebitis Pack, and a nonhormonal back-up method of birth control should be Thrombophlebitis Pack during those 7 days.
The patient begins her next and all subsequent courses of tablets on the day after taking her last light-green tablet. She should follow the same dosing schedule: If in any cycle the patient starts tablets later than the proper day, she should protect herself against pregnancy by using a nonhormonal back-up method of birth control until she has taken a pink tablet daily for 7 consecutive days.
When the patient is switching from a day regimen of tablets, she should wait 7 days after her last tablet before she starts ALESSE levonorgestrel and ethinyl estradiol.
She will probably experience withdrawal bleeding during that week. She should be sure that no more than 7 days pass after her previous day regimen. When the patient is switching from a day regimen of Behandlung von Krampfadern Behandlungsvorgang, she should start her first pack of ALESSE levonorgestrel and ethinyl estradiol on the day after her last tablet.
She should not wait any days between packs. The patient may switch any day from a progestin-only pill and should begin ALESSE levonorgestrel and ethinyl estradiol the next day. If switching from an implant or injection, the patient should start ALESSE levonorgestrel and ethinyl estradiol on the day of implant removal or, if using an injection, the day the next injection would be due. In switching from a progestin-only pill, injection, or implant, the patient should be advised to use a nonhormonal back-up method of birth control for the first 7 days of tablet-taking.
If spotting or breakthrough bleeding occur, the patient is instructed to continue on the same regimen. This Thrombophlebitis Pack of bleeding is usually transient and without significance; however, if the bleeding is persistent or prolonged, Thrombophlebitis Pack, the patient is advised to consult Krampfadern und Beingeschwüre mit Volksmedizin behandelt physician.
While there is little likelihood of ovulation occurring if only one or two pink tablets are missed, the possibility of ovulation increases with each successive day that scheduled pink tablets are missed. Although the occurrence of pregnancy is unlikely if ALESSE levonorgestrel and ethinyl estradiol is taken according to directions, if withdrawal bleeding does not occur, the possibility of pregnancy Thrombophlebitis Pack be considered, Thrombophlebitis Pack.
If the patient has not adhered to the prescribed schedule missed one or more tablets or started taking them on a day later than she should havethe probability of pregnancy should be considered at the time of the first missed period and appropriate diagnostic measures taken.
If the patient has adhered to the prescribed regimen and misses two consecutive periods, pregnancy should be ruled out. The risk of pregnancy increases with each active pink tablet missed, Thrombophlebitis Pack. The patient should be advised to use a non-hormonal back-up method for the first 7 days of tablet taking.
ALESSE levonorgestrel and ethinyl estradiol may be initiated immediately Thrombophlebitis Pack a first trimester abortion or miscarriage. An increased risk of the following serious adverse reactions see WARNINGS section for additional information has been associated with the Thrombophlebitis Pack of oral contraceptives: Thromboembolic and thrombotic disorders and other vascular problems Thrombophlebitis Pack thrombophlebitis and venous thrombosis with or without pulmonary embolism, mesenteric thrombosis, arterial thromboembolism, myocardial infarctionThrombophlebitis Pack, cerebral hemorrhage, cerebral thrombosiscarcinoma of the reproductive organs and breasts, hepatic neoplasia Thrombophlebitis Pack hepatic adenomas or benign liver tumorsocular lesions including retinal vascular thrombosisgallbladder disease, carbohydrate and lipid effects, elevated blood pressureand headache including migraine.
The following adverse reactions have been reported in patients receiving oral contraceptives and are believed to be drug related alphabetically listed:. Cataracts Cystitis-like syndrome Dysmenorrhea Hemolytic uremic syndrome Hemorrhagic eruption Optic neuritis, which may lead to partial or complete loss of vision Premenstrual syndrome Renal function, impaired.
Contraceptive effectiveness may be reduced when hormonal contraceptives are coadministered with antibiotics, anticonvulsants, and other drugs that increase the metabolism of contraceptive steroids.
This could result in unintended pregnancy or breakthrough bleeding. Examples include rifampin, rifabutin, barbiturates, primidone, phenylbutazone, phenytoin, dexamethasone, carbamazepine, felbamate, Thrombophlebitis Pack, oxcarbazepine, topiramate, griseofulvin, and modafinil, Thrombophlebitis Pack.
In such cases a back-up nonhormonal method of birth control should be considered, Thrombophlebitis Pack. Several cases of contraceptive failure and breakthrough bleeding have been reported in Thrombophlebitis Pack literature with concomitant administration of antibiotics such as ampicillin and other penicillins, and tetracyclines.
However, clinical pharmacology studies investigating drug interactions between combined oral contraceptives and these antibiotics have reported inconsistent results. Several of the anti-HIV protease inhibitors have been studied with co-administration of oral combination hormonal contraceptives; significant changes increase and decrease in the plasma levels of the estrogen and progestin have been noted in some cases.
The safety and efficacy of oral contraceptive products may be affected with coadministration of anti-HIV protease inhibitors. Healthcare providers should refer to the label of Thrombophlebitis Pack individual anti-HIV protease inhibitors for further drug-drug interaction information. Herbal products containing St. John's Wort Hypericum Thrombophlebitis Pack may induce hepatic enzymes cytochrome P and p-glycoprotein transporter and may reduce the effectiveness of contraceptive steroids.
This may also Thrombophlebitis Pack in breakthrough bleeding. Ascorbic acid and acetaminophen increase the bioavailability of ethinyl estradiol since these drugs act as competitive inhibitors for sulfation of ethinyl estradiol in the gastrointestinal wall, a known pathway of elimination for ethinyl estradiol, Thrombophlebitis Pack.
CYP 3A4 inhibitors such as indinavir, itraconazole, ketoconazole, fluconazole, and troleandomycin may increase plasma hormone levels. Troleandomycin may also increase the Thrombophlebitis Pack of intrahepatic cholestasis during coadministration with combination oral contraceptives.
Combination hormonal contraceptives containing some synthetic estrogens eg, ethinyl estradiol may inhibit the metabolism of other compounds.
Increased plasma concentrations of cyclosporin, prednisolone and other corticosteroids, and theophylline have been reported with concomitant administration of oral contraceptives.
Decreased plasma concentrations of acetaminophen and increased clearance of temazepam, salicylic acidmorphineand clofibric acid, due to induction of conjugation particularly glucuronidationThrombophlebitis Pack, have been noted when these drugs were administered with oral contraceptives.
The prescribing information of concomitant medications should be consulted to identify potential interactions. Certain endocrine- and liver-function tests and blood components may be affected by oral contraceptives:. Cigarette smoking increases the risk of serious cardiovascular side effects from oralcontraceptive use. This risk increases with age and with the extent of smoking in epidemiologic studies, 15 or more cigarettes per day was associated with a significantly increased risk and is quite marked in women over 35 years of age, Thrombophlebitis Pack.
Women who use oral contraceptives should be strongly advised not to smoke. The use of oral contraceptives is associated with increased risks of several serious conditions including venous and arterial thrombotic and thromboembolic events such as myocardial infarctionthromboembolismand Thrombophlebitis Packhepatic neoplasiagallbladder disease, and hypertensionalthough the risk of serious morbidity or mortality is very small in healthy women without underlying risk factors.
Practitioners prescribing oral contraceptives should be familiar with the following information relating to these risks. The information contained in this package insert is principally based on studies carried out in patients who used oral contraceptives with higher doses of estrogens and progestogens than those in common use today.
The effect of long-term use of the oral contraceptives Thrombophlebitis Pack lower doses of both estrogens and progestogens remains to be determined. Throughout this labeling, epidemiological studies reported are of two types: Case control studies provide a measure of the relative risk of disease, Thrombophlebitis Pack, namely, a ratio of the incidence of a disease among oral-contraceptive users to that among nonusers, Thrombophlebitis Pack.
The relative risk does not provide information on the actual clinical occurrence of a disease. Cohort studies provide a measure of Thrombophlebitis Pack risk, which is the difference in the incidence of disease between oral-contraceptive users and nonusers. The attributable risk does provide information about the actual occurrence of a disease in the population, Thrombophlebitis Pack. For further information, the reader is referred to a text on epidemiological methods.
An increased risk of myocardial infarction has been attributed to oral-contraceptive use. This risk is primarily in smokers or women with other underlying risk factors for coronary-artery disease such as hypertension, hypercholesterolemiamorbid obesity, Thrombophlebitis Pack diabetes, Thrombophlebitis Pack.
The relative risk of heart attack for current oral-contraceptive users has been estimated to be two to six. The risk is very low under the age of Smoking in combination with oral-contraceptive use has been shown to contribute substantially to the incidence of myocardial infarction in women in their mid-thirties or older with smoking accounting for the majority of excess cases. Mortality rates associated with circulatory disease have been shown to increase substantially in smokers over the age of 35 and nonsmokers over the age of 40 FIGURE II among women who use oral contraceptives.
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A Baker's cyst, also known as a popliteal cyst, is a benign swelling of the semimembranosus or more rarely some other synovial bursa found behind the knee joint.
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A Baker's cyst, also known as a popliteal cyst, is a benign swelling of the semimembranosus or more rarely some other synovial bursa found behind the knee joint.
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Fibrovein %. Each ml solution for injection contains 30mg Sodium Tetradecyl Sulfate. Each 2ml ampoule contains 60mg Sodium Tetradecyl Sulfate.
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The soleus muscle can contribute to heel, ankle, calf, low back, pain. Trigger point in this muscle can mimic temporal mandibular joint dysfunction pain.
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Junel official prescribing information for healthcare professionals. Includes: indications, dosage, adverse reactions, pharmacology and more.