Kabikinase Ketamine Hydrochloride Ketazolam Ketoconazole except Ketoconozole 1% Shampoo ; Ketoprofen Ketotifen and its salts L Labetalol Hydrochloride Lacidipine Lactulose Lamivudine Lamotrigine Lanatoside Lansoprazole Latamoxef Latanaprost Letrozole Leucovorin Calcium Leuprolide acetate Levamisole Levamisole Rafoxanide Levamphetamine and its salts Levobunolol Levocabastine Hydrochloride Levodopa and its salts Levonordefrin and its salts Levonorgestrel in doses exceeding 750mcg per tablet and when used as a post-coital contraceptive or for purposes other than contraception. Lidoflazine Liothyronine and its salts Lipase Amylase Protease Lisinopril & Hydrochlorthiazole Lisinopril and its salts Lisuride Hydrogen M aleate Lithium and its salts Lodoxamide tromethamine Lomefloxacin Lomustine Loperamide and its salts Loracarbef Lorazepam Lormetazepam Lorsartan Potassium Lorsartan Potassium Hydrochlorthiazole Lorotidine except Lorotidine 10mg tablets ; Lorotidine & Pseudoephedrine Lovastatin Loxaine and its salts L Thyroxine Sodium Lufenuron Lypressin M M afenide and its salts M annitol M aprotiline and its salts M azindol M ebanazine.
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The 1962 amendments to the Food, Drug, and Cosmetic Act, which charged the Food and Drug Administration FDA ; with regulating pharmaceutical effectiveness in addition to regulating safety, also transferred responsibility for prescription drug advertising from the Federal Trade Commission which still regulates advertising for over-the-counter drugs ; to the FDA. In the early 1980s, a few pharmaceutical manufacturers experimented with prescription drug ads directed at consumers.1 In September 1982, having previously announced that direct-to-consumer DTC ; advertising was not inherently in violation of FDA law and regulations, the FDA declared a "moratorium" on DTC advertising, with which the industry complied. In 1985, the FDA lifted its moratorium but emphasized that DTC ads must meet the same standards as those aimed at professionals. Print ads would have to include a detailed "brief summary" of risk and other information. Broadcast ads would have to include a much shorter but nonetheless lengthy "major statement" of risks, while also making "adequate provision" for viewers to obtain full FDA-approved prescribing information. Because meeting the broadcast requirements was impractical, advertisements were forced to take one of two very different approaches. "Help-seeking" ads could discuss the fact that a treatment existed for a condition, but could neither mention a drug by name nor make suggestions and representations about drug treatments. "Reminder" ads could emphasize drug brands but could not mention what conditions the drugs could treat. Under these constraints, DTC advertising gradually increased from $12 million in 1989 to $55 million in 1991, $164 million in 1993, $340 million in 1995, and $579 million in 1996 Pines 1999 ; . In August 1997, the FDA issued a preliminary "Guidance for Industry" that reinterpreted FDA regulations without actually changing any regulations.
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The main active chemical in marijuana is delta-9-tetrahydrocannabinol, or THC. It also contains more than 400 other chemicals. THC binds to nerve cells in the hippocampus of the brain, which controls learning and memory and integrates the senses with emotions and motivations. THC changes the way sensory information is processed by the hippocampus. All of this means there's a major break between what a pot user senses and what he does about it. The effects of marijuana vary a lot. Marijuana has no effect on some people. Others simply fall asleep. The effects that abusers are seeking include relaxation and giddiness. Pot smokers laugh at anything--funny or not. Many users feel dizzy, have difficulty walking, and have red, bloodshot eyes. Terrible thirst--"cotton mouth"--and hunger--"the munchies"--are typical. Many abusers feel anxious or paranoid every time they use the drug and lyrica.
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ELIGIBILITY .14 EMPLOYEE ELIGIBILITY .14 DEPENDENT ELIGIBILITY .14 ENROLLMENT.15 REGULAR ENROLLMENT .15 SPECIAL ENROLLMENT FOR LOSS OF OTHER COVERAGE .16 SPECIAL ENROLLMENT FOR LOSS OF ELIGIBILITY DUE TO REACHING LIFETIME MAXIMUM BENEFITS .16 SPECIAL ENROLLMENT FOR NEW DEPENDENTS .17 SPECIAL ENROLLMENT FOR NEW DEPENDENTS THROUGH QUALIFIED MEDICAL CHILD SUPPORT ORDER: .17 OPEN ENROLLMENT .17 EFFECTIVE DATE OF COVERAGE.18 EMPLOYEE EFFECTIVE DATE .18 DEPENDENT EFFECTIVE DATE .18 TERMINATION OF COVERAGE .18 EMPLOYEE .18 DEPENDENT S ; .19 POSTPONEMENT OF TERMINATION IN CASES OF DISABILITY .19 POSTPONEMENT OF TERMINATION IN CASES OF CONTINUOUS CONFINEMENT .20 CERTIFICATE OF CREDITABLE COVERAGE .20 APPROVED FAMILY AND MEDICAL LEAVE .20 APPROVED LEAVE OF ABSENCE OTHER THAN FEDERAL FAMILY AND MEDICAL LEAVE OF ABSENCE ; .21 REINSTATEMENT OF COVERAGE .21 SELF-PAYMENT IN THE EVENT OF A LABOR DISPUTE .21 and
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Table 1. Enrollment Characteristics of Cases With Any Nelfinavir Exposure During Pregnancy Pregnancies enrolled N 944, 91.7% ; Year of enrollment 1997 1998 1999 Age y ; Mean standard error ; Median interquartile range ; Minimummaximum Missing Race White Black Hispanic Other Unknown CD4 cell count at start of pregnancy 200 mm3 200499 mm3 500 mm3 Missing Clinical categories at start of pregnancy Asymptomatic, acute primary ; HIV Symptomatic AIDS-indicator conditions HIV postexposure prophylaxis Unknown 35 3.7 ; 125 13.2 ; 157 16.6 ; 276 29.2 ; 316 33.5 ; 35 3.7 ; 28.1 0.2 ; 28.0 9.0 ; 1543 4 187 ; 504 53.4 ; 197 20.9 ; 38 4.0 ; 18 1.9 ; 211 22.4 ; 462 48.9 ; 249 26.4 ; 22 2.3 ; 679 71.9 ; 109 11.5 ; 124 13.1 ; 3 ; 29 3.0 ; Lost to follow-up N 85, 8.3% ; 3 3.5 ; 23 27.1 ; 22 25.9 ; 22 25.9 ; 15 17.6 ; 0 27.5 0.6 ; 27.0 8.0 ; 1639 2 18 ; 39 45.9 ; 15 17.6 ; 3 3.6 ; 10 11.8 ; 14 16.5 ; 37 43.5 ; 24 28.2 ; 10 11.8 ; 50 58.8 ; 10 11.8 ; 11 12.9 ; 1 1.2 ; 13 15.3.
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Excluding Injectables Therapeutic Effective Drug Name Classification Date ZYPREXA ZYDIS 9 05 H7T H7U - ANTIPSYCHOTICS, DOPAMINE & SEROTONIN ANTAGONISTS LOXAPINE H7U LOXAPINE SUCCINATE H7U LOXITANE C H7U H7X - ANTIPSYCHOTICS, ATYPICAL, DOPAMINE PARTIAL AGONIST ABILIFY H7X H7Y - TX FOR ATTENTION DEFICIT-HYPERACT. ADHD ; , NRI-TYPE STRATTERA 7 1 06 H7Y H7Z - SSRI &ANTIPSYCH, ATYP, DOPAMINE & SEROTONIN ANTAG COMB 7 11 05 SYMBYAX H7Z J1A - PARASYMPATHETIC AGENTS BETHANECHOL CHLORIDE 1 11 06 J1A EVOXAC J1A PILOCARPINE HCL 4 1 07 J1A SALAGEN 4 1 07 J1A J1B - CHOLINESTERASE INHIBITORS ARICEPT J1B ARICEPT ODT 10 1 05 J1B EXELON J1B PROSTIGMIN J1B RAZADYNE 10 1 05 * J1B RAZADYNE ER 10 1 J1B J2A - BELLADONNA ALKALOIDS BELLADONNA W PHENOBARBITAL J2A HYOSCYAMINE J2A HYOSCYAMINE SULFATE J2A J2B - ANTICHOLINERGICS, QUATERNARY AMMONIUM CANTIL J2B PROPANTHELINE BROMIDE J2B ROBINUL J2B ROBINUL FORTE J2B J2D - ANTICHOLINERGICS ANTISPASMODICS DICYCLOMINE HCL J2D J3A - SMOKING DETERRENT AGENTS GANGLIONIC STIM, OTHERS ; NICODERM CQ 1 11 J3A NICORELIEF 1 11 06 J3A NICOTINE J3A NICOTINE GUM & PATCHES 1 11 06 J3A NICOTINE POLACRILEX 1 11 06 J3A NICOTINE TRANSDERMAL J3A NTS 1 11 06 J3A ZYBAN J3A.
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D. None of the following complications or contraindications are present: 1. History of clozapine-induced leukopenia, agranulocytosis or granuloctyopenia 2. Medical condition or drug associated with myeloproliferative disease or immunosuppression 3. Severe medical condition, or other illnesses causing central nervous system depression or concurrent organic state 4. Poor medical compliance and or poor compliance with lab testing 5. Initial WBC 3500 mm3 or neutrophil 2000 mm3 ; 6. History of hypersensitivity to a clozapine related drug amoxapine, loxxapine ; 7. History of significant physical illness in the prior month 8. History of blood disorders E. The following potential concerns and complications have been addressed, if applicable: 1. Presence of concurrent active substance abuse 2. History of seizure disorder, or neurological illness i. Finnish or Jewish background, especially Ashkenazi Jew ii. Laboratory or clinical evident of significant hepatic, renal, or cardiopulmonary disease iii. Unexplained abnormalities in laboratory tests within the preceding four weeks iv. Prostatic enlargement or narrow angle glaucoma v. Need for continued use of heterocyclic or MAOI-type antidepressants vi. Concomitant use of see Table #1, page 35 ; : a. Bone marrow suppressants b. Antihypertensive agents c. CNS depressants d. Highly protein bound drugs e. Substrates inhibitors inducers of CYP 1A2, 2D6, and 3A4 vii. History of orthostatic hypotension F. Clozapine Monitoring Committee Application Form attachment #1 ; completion and approval. III. Initiation of Clozapine Treatment The following must be completed if the patient is approved for clozapine administration: 1. Physician must be registered as a provider with the National Registry by calling the National Registry or providing the completed forms to the registry. 2. Physician will explain medication to the patient and have patient sign Informed Consent for Clozapine. 3. Physician calls the National Registry to obtain rechallenge clearance authorization. A patient number is received from the National Registry, and documented in the client Medical Record. Telephone Numbers Clozaril Novartis ; Patient Registry Clozapine IVAX ; Patient Registry 800 ; 448-5938 800 ; 507-8334 FAX 800 ; 648-6015 FAX 800 ; 507-8339 and lovastatin.
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