WARNINGS SECTION.

WARNINGS. The potential for development of acute PJP still exists in patients receiving Pentamidine Isethionate prophylaxis. Therefore, any patient with symptoms suggestive of the presence of pulmonary infection, including but not limited to dyspnea, fever or cough, should receive thorough medical evaluation and appropriate diagnostic tests for possible acute PJP as well as for other opportunistic and nonopportunistic pathogens. The use of Pentamidine Isethionate may alter the clinical and radiographic features of PJP and could result in an atypical presentation, including but not limited to mild disease or focal infection.Prior to initiating Pentamidine Isethionate prophylaxis, symptomatic patients should be evaluated appropriately to exclude the presence of PJP. The recommended dose of Pentamidine Isethionate for the prevention of PJP is insufficient to treat acute PJP.

GENERAL PRECAUTIONS SECTION.

General. The extent and consequence of pentamidine accumulation following chronic inhalation therapy are not known. As result, patients receiving Pentamidine Isethionate should be closely monitored for the development of serious adverse reactions that have occurred in patients receiving parenteral pentamidine, including hypotension, hypoglycemia, hyperglycemia, hypocalcemia, anemia, thrombocytopenia, leukopenia, hepatic or renal dysfunction, ventricular tachycardia, pancreatitis, Stevens-Johnson syndrome, hyperkalemia and abnormal ST segment of ECG.Extrapulmonary infection with P. jiroveci has been reported infrequently. Most, but not all, of the cases have been reported in patients who have history of PJP. The presence of extrapulmonary pneumocystosis should be considered when evaluating patients with unexplained signs and symptoms.Cases of acute pancreatitis have been reported in patients receiving aerosolized pentamidine. Pentamidine Isethionate should be discontinued if signs or symptoms of acute pancreatitis develop.

ADVERSE REACTIONS SECTION.

ADVERSE REACTIONS. The most frequently reported unsolicited adverse events (1 to 5%) in clinical trials, regardless of their relation to Pentamidine Isethionate therapy were as follows (n=931):Body as Whole: Night sweats.Gastrointestinal: Diarrhea and nausea.Hematologic: Anemia.Infection: Bronchitis, non-specific herpes, herpes zoster, non-specific influenza, oral Candida, pharyngitis, sinusitis, and upper respiratory tract.Nervous System: Headache.Respiratory System: Chest pain, cough, and wheezing.Special Senses: Bad taste.Adverse events of less than 1% incidence were as follows (No causal relationship to treatment has been established for these adverse events):Body as Whole: Allergic reaction, non-specific allergy, body odor, facial edema, fever, leg edema, lethargy, low body temperature, and temperature abnormality.Cardiovascular: Cerebrovascular accident, hypotension, hypertension, palpitations, poor circulation, syncope, tachycardia, vasodilatation and vasculitis.Gastrointestinal: Abdominal cramps, abdominal pain, constipation, dry mouth, dyspepsia, gastritis, gastric ulcer, gingivitis, hiatal hernia, hypersalivation, oral ulcer/abscess, splenomegaly, and vomiting.Hematological: Eosinophilia, neutropenia, non-specific cytopenia, pancytopenia, and thrombocytopenia.Hepatic: Hepatitis, hepatomegaly, and hepatic dysfunction.Infection: Bacterial pneumonia, central venous line related sepsis, cryptococcal meningitis, cytomegalovirus (CMV) colitis, CMV retinitis, esophageal Candida, histoplasmosis, Kaposis sarcoma, non-specific mycoplasma, oral herpes, non-specific otitis, non-specific pharyngitis, pharyngeal herpes, non-specific serious infection, tonsillitis, tuberculosis, and viral encephalitis.Metabolic: Hyperglycemia, hypoglycemia, and hypocalcemia.Musculoskeletal: Arthralgia, gout, and myalgia.Neurological: Anxiety, confusion, depression, drowsiness, emotional lability, hallucination, hypesthesia, insomnia, memory loss, neuralgia, neuropathy, non-specific neuropathy, nervousness, paranoia, paresthesia, peripheral neuropathy, seizure, tremors, unsteady gait, and vertigo.Reproductive: Miscarriage.Respiratory system: Asthma, bronchitis, bronchospasm, chest congestion, chest tightness, coryza, cyanosis, eosinophilic or interstitial pneumonitis, gagging, hemoptysis, hyperventilation, laryngitis, laryngospasm, non-specific lung disorder, nasal congestion, pleuritis, pneumothorax, rales, rhinitis, shortness of breath, non-specific sputum, and tachypnea.Skin: Desquamation, dry and breaking hair, dry skin, erythema, non-specific dermatitis, pruritus, rash, and urticaria.Special senses: Blepharitis, blurred vision, conjunctivitis, contact lens discomfort, eye pain or discomfort, hemianopsia, loss of taste, non-specific odor, and smell.Urogenital: Flank pain, incontinence, nephritis, renal failure, and renal pain.In clinical trial where some adverse events were solicited by investigators, the incidences were as follows:Cough (62.7%)Decreased appetite (50.0%)Dizziness or light-headedness (45.1%)Fatigue (65.7%)Fever (51.0%)Non-specific serious infection (15.2%)Shortness of breath (48.3%)Wheezing (32.4%)From post-marketing clinical experience with Pentamidine Isethionate the following spontaneous adverse events have been reported: anaphylaxis, colitis, diabetes, dyspnea, esophagitis, hematochezia, increased blood urea nitrogen (BUN) and serum creatinine levels, melena, pancreatitis (see WARNINGS), syndrome of inappropriate antidiuretic hormone (SIADH), and torsade de pointes.

CLINICAL PHARMACOLOGY SECTION.

CLINICAL PHARMACOLOGY. Microbiology. Mechanism of Action. Studies suggest that the pentamidine isethionate interferes with microbial nuclear metabolism by inhibition of DNA, RNA, phospholipid and protein synthesis. However, the mode of action is not fully understood.. Activity in vitro and in vivo. Pentamidine isethionate, an aromatic diamidine, is known to have activity against Pneumocystis jiroveci.. Pharmacokinetics. In AIDS patients with suspected Pneumocystis jiroveci pneumonia (PJP), the mean concentrations of pentamidine determined 18 to 24 hours after inhalation therapy were 23.2 ng/mL (range 5.1 to 43.0 ng/mL) in bronchoalveolar lavage fluid and 705 ng/mL (range 140 to 1336 ng/mL) in sediment after administration of 300 mg single dose via the Respirgard(R) II nebulizer. In AIDS patients with suspected PJP, the mean concentrations of pentamidine determined 18 to 24 hours after 4 mg/kg intravenous dose were 2.6 ng/mL (range 1.5 to 4.0 ng/mL) in bronchoalveolar lavage fluid and 9.3 ng/mL (range 6.9 to 12.8 ng/mL) in sediment. In the patients who received aerosolized pentamidine, the peak plasma levels of pentamidine were at or below the lower limit of detection of the assay (2.3 ng/mL).Following single 2-hour intravenous infusion of mg/kg of pentamidine isethionate to AIDS patients, the mean plasma Cmax, 1/2 and clearance were 612 +- 371 ng/mL, 6.4 +- 1.3 hr and 248 +- 91 L/hr respectively. In another study of aerosolized pentamidine in 13 AIDS patients with acute PJP who received mg/kg/day administered via the Ultra Vent(R) jet nebulizer, peak plasma levels of pentamidine averaged 18.8 +- 11.9 ng/mL after the first dose. During the next 14 days of repeated dosing, the highest observed Cmax averaged 20.5 +- 21.2 ng/mL. In third study, following daily administration of 600 mg of inhaled pentamidine isethionate with the Respirgard(R) II nebulizer for 21 days in 11 patients with acute PJP, mean plasma levels measured shortly after the 21st dose averaged 11.8 +- 10.0 ng/mL. Plasma concentrations after aerosol administration are substantially lower than those observed after comparable intravenous dose. The extent of pentamidine accumulation and distribution following chronic inhalation therapy are not known.In rats, intravenous administration of 5 mg/kg dose resulted in concentrations of pentamidine in the liver and kidney that were 87.5 and 62.3-fold higher, respectively, than levels in those organs following mg/kg administered as an aerosol.No pharmacokinetic data are available following aerosol administration of pentamidine in humans with impaired hepatic or renal function.

DOSAGE & ADMINISTRATION SECTION.

DOSAGE AND ADMINISTRATION. IMPORTANT: PENTAMIDINE ISETHIONATE MUST BE DISSOLVED ONLY IN STERILE WATER FOR INJECTION, USP. DO NOT USE SALINE SOLUTION FOR RECONSTITUTION BECAUSE THE DRUG WILL PRECIPITATE. DO NOT MIX THE Pentamidine Isethionate SOLUTION WITH ANY OTHER DRUGS. DO NOT USE THE RESPIRGARD(R) II NEBULIZER TO ADMINISTER BRONCHODILATOR.. Reconstitution. The contents of one vial (300 mg) must be dissolved in mL Sterile Water for Injection, USP. Place the entire reconstituted contents of the vial into the Respirgard(R) II nebulizer reservoir for administration.. Dosage. The recommended adult dosage of Pentamidine Isethionate for the prevention of Pneumocystis jiroveci pneumonia is 300 mg once every four weeks administered via the Respirgard(R) II nebulizer.The dose should be delivered until the nebulizer chamber is empty (approximately 30 to 45 minutes). The flow rate should be to liters per minute from 40 to 50 pounds per square inch (PSI) air or oxygen source. Alternatively, 40 to 50 PSI air compressor can be used with flow limited by setting the flowmeter at to liters per minute or by setting the pressure at 22 to 25 PSI. Low pressure (less than 20 PSI) compressors should not be used.. Stability. Freshly prepared solutions for aerosol use are recommended. After reconstitution with sterile water, the Pentamidine Isethionate solution is stable for 48 hours in the original vial at room temperature if protected from light.

INDICATIONS & USAGE SECTION.

INDICATIONS AND USAGE. Pentamidine Isethionate is indicated for the prevention of Pneumocystis jiroveci pneumonia (PJP) in high-risk, HIV-infected patients defined by one or both of the following criteria:i. history of one or more episodes of PJPii. peripheral CD4+ (T4 helper/inducer) lymphocyte count less than or equal to 200/mm3.These indications are based on the results of an 18-month randomized, dose-response trial in high risk HIV-infected patients and on existing epidemiological data from natural history studies.The patient population of the controlled trial consisted of 408 patients, 237 of whom had history of one or more episodes of PJP. The remaining patients without history of PJP included 55 patients with Kaposis sarcoma and 116 patients with other AIDS diagnoses, ARC or asymptomatic HIV infection. Patients were randomly assigned to receive Pentamidine Isethionate via the Respirgard(R) II nebulizer at one of the following three doses: 30 mg every two weeks (n=135), 150 mg every two weeks (n=134) or 300 mg every four weeks (n=139). The results of the trial demonstrated significant protective effect (p<0.01) against PJP with the 300 mg every four week dosage regimen compared to the 30 mg every two week dosage regimen. The 300 mg dose regimen reduced the risk of developing PJP by 50 to 70% compared to the 30 mg regimen. total of 293 patients (72% of all patients) also received zidovudine at some time during the trial. The analysis of the data demonstrated the efficacy of the 300 mg dose even after adjusting for the effect of zidovudine.The results of the trial further demonstrate that the dose and frequency of dosing are important to the efficacy of Pentamidine Isethionate prophylaxis in that multiple analyses consistently demonstrated trend toward greater efficacy with 300 mg every four weeks as compared to 150 mg every two weeks.No dose-response was observed for reduction in overall mortality; however, mortality from PJP was low in all three dosage groups.

PHARMACOKINETICS SECTION.

Pharmacokinetics. In AIDS patients with suspected Pneumocystis jiroveci pneumonia (PJP), the mean concentrations of pentamidine determined 18 to 24 hours after inhalation therapy were 23.2 ng/mL (range 5.1 to 43.0 ng/mL) in bronchoalveolar lavage fluid and 705 ng/mL (range 140 to 1336 ng/mL) in sediment after administration of 300 mg single dose via the Respirgard(R) II nebulizer. In AIDS patients with suspected PJP, the mean concentrations of pentamidine determined 18 to 24 hours after 4 mg/kg intravenous dose were 2.6 ng/mL (range 1.5 to 4.0 ng/mL) in bronchoalveolar lavage fluid and 9.3 ng/mL (range 6.9 to 12.8 ng/mL) in sediment. In the patients who received aerosolized pentamidine, the peak plasma levels of pentamidine were at or below the lower limit of detection of the assay (2.3 ng/mL).Following single 2-hour intravenous infusion of mg/kg of pentamidine isethionate to AIDS patients, the mean plasma Cmax, 1/2 and clearance were 612 +- 371 ng/mL, 6.4 +- 1.3 hr and 248 +- 91 L/hr respectively. In another study of aerosolized pentamidine in 13 AIDS patients with acute PJP who received mg/kg/day administered via the Ultra Vent(R) jet nebulizer, peak plasma levels of pentamidine averaged 18.8 +- 11.9 ng/mL after the first dose. During the next 14 days of repeated dosing, the highest observed Cmax averaged 20.5 +- 21.2 ng/mL. In third study, following daily administration of 600 mg of inhaled pentamidine isethionate with the Respirgard(R) II nebulizer for 21 days in 11 patients with acute PJP, mean plasma levels measured shortly after the 21st dose averaged 11.8 +- 10.0 ng/mL. Plasma concentrations after aerosol administration are substantially lower than those observed after comparable intravenous dose. The extent of pentamidine accumulation and distribution following chronic inhalation therapy are not known.In rats, intravenous administration of 5 mg/kg dose resulted in concentrations of pentamidine in the liver and kidney that were 87.5 and 62.3-fold higher, respectively, than levels in those organs following mg/kg administered as an aerosol.No pharmacokinetic data are available following aerosol administration of pentamidine in humans with impaired hepatic or renal function.

PRECAUTIONS SECTION.

PRECAUTIONS. IMPORTANT: DO NOT MIX THE Pentamidine Isethionate SOLUTION WITH ANY OTHER DRUGS. DO NOT USE THE RESPIRGARD(R) II NEBULIZER TO ADMINISTER BRONCHODILATOR.(See DOSAGE AND ADMINISTRATION).. Pulmonary. Inhalation of Pentamidine Isethionate may induce bronchospasm or cough. This has been noted particularly in some patients who have history of smoking or asthma. In clinical trials, cough and bronchospasm were the most frequently reported adverse experiences associated with Pentamidine Isethionate administration (38% and 15%, respectively of patients receiving the 300 mg dose); however less than 1% of the doses were interrupted or terminated due to these effects. For the majority of patients, cough and bronchospasm were controlled by administration of an aerosolized bronchodilator (only 1% of patients withdrew from the study due to treatment-associated cough or bronchospasm). In patients who experience bronchospasm or cough, administration of an inhaled bronchodilator prior to giving each Pentamidine Isethionate dose may minimize recurrence of the symptoms.. General. The extent and consequence of pentamidine accumulation following chronic inhalation therapy are not known. As result, patients receiving Pentamidine Isethionate should be closely monitored for the development of serious adverse reactions that have occurred in patients receiving parenteral pentamidine, including hypotension, hypoglycemia, hyperglycemia, hypocalcemia, anemia, thrombocytopenia, leukopenia, hepatic or renal dysfunction, ventricular tachycardia, pancreatitis, Stevens-Johnson syndrome, hyperkalemia and abnormal ST segment of ECG.Extrapulmonary infection with P. jiroveci has been reported infrequently. Most, but not all, of the cases have been reported in patients who have history of PJP. The presence of extrapulmonary pneumocystosis should be considered when evaluating patients with unexplained signs and symptoms.Cases of acute pancreatitis have been reported in patients receiving aerosolized pentamidine. Pentamidine Isethionate should be discontinued if signs or symptoms of acute pancreatitis develop.. Drug Interactions. While specific studies on drug interactions with Pentamidine Isethionate have not been conducted, the majority of patients in clinical trials received concomitant medications, including zidovudine, with no reported interactions. Because the nephrotoxic effects may be additive, the concomitant or sequential use of Pentamidine Isethionate and other nephrotoxic drugs such as aminoglycosides, amphotericin B, cisplatin, foscarnet, or vancomycin should be closely monitored and avoided, if possible.. Carcinogenesis, Mutagenesis and Impairment of Fertility. Literature reports indicate that pentamidine was not mutagenic in the Ames bacterial (S. typhimurium) test and did not induce an increase in chromosomal aberrations in Chinese Hamster Ovary (CHO) cell or in human lymphocytes in vitro.No studies have been conducted to determine effects of pentamidine isethionate on carcinogenicity or fertility.. Pregnancy-Pregnancy Category C. There are no adequate and well controlled studies of Pentamidine Isethionate in pregnant women. literature report indicated that intravenously administered pentamidine in pregnant rats at mg/kg/day was embryolethal; teratogenicity was not observed in this study. It is unknown whether pentamidine administered via the aerosolized route crosses the placenta at clinically significant concentrations. It is not known whether Pentamidine Isethionate can cause fetal harm when administered to pregnant woman. Pentamidine Isethionate should be given to pregnant woman only if clearly needed.. Nursing Mothers. It is not known whether Pentamidine Isethionate is excreted in human milk. Because of the potential for serious adverse reactions in nursing infants from Pentamidine Isethionate, decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother. Because many drugs are excreted in human milk, Pentamidine Isethionate should not be given to nursing mother unless the potential benefits are judged to outweigh the unknown risks.. Pediatric Use. The safety and effectiveness of Pentamidine Isethionate in pediatric patients (birth to 16 years of age) have not been established.

SPL UNCLASSIFIED SECTION.

Activity in vitro and in vivo. Pentamidine isethionate, an aromatic diamidine, is known to have activity against Pneumocystis jiroveci.. Pharmacokinetics. In AIDS patients with suspected Pneumocystis jiroveci pneumonia (PJP), the mean concentrations of pentamidine determined 18 to 24 hours after inhalation therapy were 23.2 ng/mL (range 5.1 to 43.0 ng/mL) in bronchoalveolar lavage fluid and 705 ng/mL (range 140 to 1336 ng/mL) in sediment after administration of 300 mg single dose via the Respirgard(R) II nebulizer. In AIDS patients with suspected PJP, the mean concentrations of pentamidine determined 18 to 24 hours after 4 mg/kg intravenous dose were 2.6 ng/mL (range 1.5 to 4.0 ng/mL) in bronchoalveolar lavage fluid and 9.3 ng/mL (range 6.9 to 12.8 ng/mL) in sediment. In the patients who received aerosolized pentamidine, the peak plasma levels of pentamidine were at or below the lower limit of detection of the assay (2.3 ng/mL).Following single 2-hour intravenous infusion of mg/kg of pentamidine isethionate to AIDS patients, the mean plasma Cmax, 1/2 and clearance were 612 +- 371 ng/mL, 6.4 +- 1.3 hr and 248 +- 91 L/hr respectively. In another study of aerosolized pentamidine in 13 AIDS patients with acute PJP who received mg/kg/day administered via the Ultra Vent(R) jet nebulizer, peak plasma levels of pentamidine averaged 18.8 +- 11.9 ng/mL after the first dose. During the next 14 days of repeated dosing, the highest observed Cmax averaged 20.5 +- 21.2 ng/mL. In third study, following daily administration of 600 mg of inhaled pentamidine isethionate with the Respirgard(R) II nebulizer for 21 days in 11 patients with acute PJP, mean plasma levels measured shortly after the 21st dose averaged 11.8 +- 10.0 ng/mL. Plasma concentrations after aerosol administration are substantially lower than those observed after comparable intravenous dose. The extent of pentamidine accumulation and distribution following chronic inhalation therapy are not known.In rats, intravenous administration of 5 mg/kg dose resulted in concentrations of pentamidine in the liver and kidney that were 87.5 and 62.3-fold higher, respectively, than levels in those organs following mg/kg administered as an aerosol.No pharmacokinetic data are available following aerosol administration of pentamidine in humans with impaired hepatic or renal function.