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DRUG TESTING PROCEDURE All specimen collection and testing for drugs shall be conducted in accordance with Sections 440.

The District may test for any or all of the following: Alcohol Amphetamines Cannabinoids Cocaine Phencyclidine Methaqualone Opiates Barbiturates Benzodiazepines Methadone Propoxyphene 2.

The initial screen for all drugs shall use an immunoassay.

The initial test for alcohol shall be an enzyme oxidation methodology. When first screening specimens, all levels equal to or exceeding the following shall be reported as positive: Alcohol . 05g% (by blood) Amphetamines 1000 ng/ml Cannabinoids 50 ng/ml Cocaine 300 ng/ml Phencyclidine 25 ng/ml Methaqualone 300 ng/ml Opiates 300 ng/ml Barbiturates 300 ng/ml Benzodiazepines children's allegra ingredients 300 ng/ml Methadone 300 ng/ml Propoxyphene 300 ng/ml These levels will remain in effect until such time as they are revised by Federal Legislation or State Statute. All new levels will become effective on the date specified within the related legislation.

All specimens identified as positive on the initial tests shall be confirmed using a second test. A gas chromatography/mass spectrometry (GC/MS) test, or an equivalent or more accurate scientifically accepted method approved by the children's allegra ingredients State or Federal government will be used children's allegra ingredients for the confirmation test for narcotics. The confirmation test for alcohol will be gas chromatography. All confirmations shall be done by quantitative analysis. When confirming children's allegra ingredients initial results, all levels equal to or exceeding the following shall be reported as positive: Alcohol . 05g% (by children's allegra ingredients blood) Amphetamines 500 ng/ml Cannabinoids 15 ng/ml Cocaine 150 ng/ml Phencyclidine 25 ng/ml Methaqualone 150 children's allegra ingredients ng/ml Opiates 300 ng/ml Barbiturates 150 ng/ml Benzodiazepines 150 ng/ml Methadone 150 ng/ml Propoxyphene 150 ng/ml These children's allegra ingredients levels will remain in effect until such time as they are revised by Federal Legislation or State Statute.

All new levels will children's allegra ingredients become effective on the date children's allegra ingredients specified within the related legislation. The laboratory shall report test results to a medical review officer (MRO) chosen by the District to act on its behalf. These children's allegra ingredients results shall be reported within children's allegra ingredients seven (7) working days after receipt of the specimen by the laboratory. The laboratory shall transmit results to the medical review officer (children's allegra ingredients MRO) in a manner designed to ensure confidentiality of the information. All records pertaining to a given specimen shall be retained by allegra d price comparison the laboratory for a minimum of two (2) years, unless the District or the employee requests that records be retained for a longer period of time. Within five (5) working days after receipt of a confirmed positive test result from the medical review officer (MRO), the Human Resources Office shall inform the employee in writing of such positive test result, the consequences of such result, and the options available to children's allegra ingredients the employee. Notification shall be via certified mail or hand-delivered. Absent extenuating circumstances, mailed notification shall be deemed received by the employee when signed for, or seven (7) calendar days after delivery, children's allegra ingredients whichever occurs first. A copy of the test results will be provided to the employee with this notification. Within five (5) working days after receiving notice of a allegra wilde new york confirmed positive test result from the Human Resources Office, the employee may submit information to the Human Resources Office explaining or contesting the test results and why the results do not constitute a allegra geller music violation of this program.



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