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Bacterial, viral and other infections due to opportunistic pathogens, includingBefore using this medication, tell your doctor or pharmacist your medical history, especially of: eye cataracts, liver disease, low white blood cell count (including history of low white blood cell count caused by medications), seizure disorder, trouble swallowing, thyroid problems, stomach/intestinal blockage (such as severe constipation, bowel obstruction), stomach/intestines that are not moving (such as ileus).

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Very common (10% or more): Depression (up to 19%), insomnia (included dreams/sleeping problems; up to 16.3%), anxiety (up to 13%)

burn-like blistering of the skin where the transdermal patch is worn;Invasive fungal infections, including hislasmosis, coccidioidomycosis, candidiasis, aspergillosis, blastomycosis, and pneumocystosis. Patients with hislasmosis or other invasive fungal infections may present with disseminated, rather than localized, disease. Antigen and antibody testing for hislasmosis may be negative in some patients with active infection. Empiric anti-fungal therapy should be considered in patients at risk for invasive fungal infections who develop severe systemic illness.Less serious side effects may include:

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potassium iodide 3) Following this 1-week waiting time, begin taking a daily tablet again for the next 20 days. dizziness


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The acellular pertussis vaccine components are produced from Bordetellapertussis cultures grown in Stainer-Scholte medium2 modified by the addition of casamino acids and dimethyl-beta-cyclodextrin. PT, FHA and PRN are isolated separately from the supernatant culture medium. The FIM components are extracted and co-purified from the bacterial cells. The pertussis antigens are purified by sequential filtration, salt-precipitation, ultrafiltration and chromatography. PT is detoxified with glutaraldehyde. FHA is treated with formaldehyde, and the residual aldehydes are removed by ultrafiltration. The individual antigens are adsorbed separately onto aluminum phosphate.nicardipine

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