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It is chronic viral hepatitis in its terminal stage and characteristic complications (esophageal and gastric bleeding, phlegmon of the gastrointestinal tract with ascites-peritonitis, etc.) that have recently become the main diseases in cases where HIV infection is considered in heading combined, competing or concomitant disease.

If a patient has infectious and / or oncological diseases, including tuberculosis (Asthma Buy Bromide) (Tiotropium - online Spiriva for 9mcg example, fibrous-cavernous, cirrhotic) before the detection of HIV infection, in the event of a death, the initial cause of death should usually be considered infectious or oncological diseases, and HIV infection may take the position of a comorbid or concomitant disease / condition (depending on the stage of HIV infection).

In the presence of conditions related to the list of AIDS markers, a mandatory indication in the diagnosis after the phase of HIV infection "AIDS" is required. All conditions related to AIDS require clear confirmation using appropriate methods and diagnosis of HIV infection. Without objective confirmation of an AIDS-indicator pathology at an autopsy (for example, if there is only a record of the attending physician in the medical records), AIDS as the cause of death is not included in the diagnosis.

Taking into account international data, all B-cell non-Hodgkin's lymphomas should also be classified as AIDS-defining diseases . To establish the concept of “pronounced immunodeficiency” and classify manifestations[1] of tuberculosis and other infectious diseases as AIDS, the laboratory criterion should be the CD4 count 25 (or body weight >75 kg).

Pregnancy. d4T** Peripheral neuropathy, lipoatrophy, or lipodystrophy Age over 40 years -1.

CD4 count ?200 µl Concurrent use of isoniazid or ddI. TDF**, AZT*[OAS3] [EC4] *, ABC** 1 after hemodialysis; 2 patient data are limited; pharmacokinetic studies have shown no need to change doses Annex G6.

Change of ARVP in the development of drug intolerance Comments: stavudine** (d4T**) can only be used at 30mg twice daily ARVP Main types of toxicity Risk factors Choice of other ARVs Lactic acidosis or severe hepatomegaly with hypersteatosis, acute pancreatitis BMI >25 (or body weight >75 kg).

Pregnancy. DRV**/r** Hepatotoxicity Underlying liver disease. Concurrent use of hepatotoxic drugs ATV**/r**, LPV/r**, AI. If DRV**/r** is part of third-line ART, options are limited.

Severe skin reactions and hypersensitivity reactions Allergy to sulfa drugs EFV** Continuous toxic effects on the central nervous system (eg, manifesting as abnormal dreams, depression, or confusion) Depression or other mental disorder (in the previous period or at the initial stage of treatment). Taking the drug during the day NVP**, ESV** If intolerant to NVP**

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  • or boosted PIs. Concurrent use of hepatotoxic drugs Convulsions History of seizures reaction , Stevens-Johnson syndrome. Potential risk of neural tube birth defects (very low risk in humans). Gynecomastia in men Risk factors unknown ETR** Severe skin reactions and hypersensitivity reactions. Unknown. Integrase inhibitors. LPV/r** Deviations from the norm electrocardiogram (prolongation of the PR and QT interval) Previous lesion of the conduction system. Concomitant use of other drugs that may prolong the PR interval. ATV**/r** or FPV**/r** or DRV**/r**.

    If boosted PIs are contraindicated and NNRTIs are ineffective, Buy Spiriva (Tiotropium integrase Bromide) 9mcg online - Asthma inhibitors should be considered QT interval prolongation Congenital long QT syndrome. Concomitant use of other drugs that may prolong the QT interval Hepatotoxicity Underlying liver disease. Concurrent use of hepatotoxic drugs pancreatitis Late stage HIV infection Risk of prematurity, lipoatrophy or metabolic syndrome, dyslipidemia, severe diarrhea Risk factors unknown NVP** Hepatotoxicity Underlying liver disease.

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