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                    [Title] => Dialysis drug reactions reach 130 cases
                    [Summary] => 
At least 130 patients nationwide who have been undergoing dialysis experienced unusual chills due to a contaminated drug, the Food and Drug Administration (FDA) reported yesterday.

                    [DatePublished] => 2014-07-12 00:00:00
                    [ColumnID] => 0
                    [Focus] => 0
                    [AuthorID] => 1097338
                    [AuthorName] =>  Mayen Jaymalin
                    [SectionName] => Metro
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                    [ArticleID] => 1339819
                    [Title] => DOH to hospitals: Report adverse reactions to dialysis drug
                    [Summary] => 
The Department of Health (DOH) urged all hospitals yesterday to report to the Food and Drug Administration (FDA) if they have patients who experienced adverse reactions to a dialysis drug.

                    [DatePublished] => 2014-06-28 00:00:00
                    [ColumnID] => 0
                    [Focus] => 0
                    [AuthorID] => 1804896
                    [AuthorName] => Sheila Crisostomo
                    [SectionName] => Metro
                    [SectionUrl] => metro
                    [URL] => 
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                    [ArticleID] => 1337206
                    [Title] => FDA bans medicine for blood clot
                    [Summary] => 
The Food and Drugs Administration (FDA) has temporarily banned the sale of a medicine used to treat blood clot from India due to reported serious adverse reactions to the drug.

                    [DatePublished] => 2014-06-21 00:00:00
                    [ColumnID] => 0
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                    [AuthorID] => 1097338
                    [AuthorName] =>  Mayen Jaymalin
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MEPARIN

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                    [ArticleID] => 1345175
                    [Title] => Dialysis drug reactions reach 130 cases
                    [Summary] => 
At least 130 patients nationwide who have been undergoing dialysis experienced unusual chills due to a contaminated drug, the Food and Drug Administration (FDA) reported yesterday.

                    [DatePublished] => 2014-07-12 00:00:00
                    [ColumnID] => 0
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                    [AuthorName] =>  Mayen Jaymalin
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                    [ArticleID] => 1339819
                    [Title] => DOH to hospitals: Report adverse reactions to dialysis drug
                    [Summary] => 
The Department of Health (DOH) urged all hospitals yesterday to report to the Food and Drug Administration (FDA) if they have patients who experienced adverse reactions to a dialysis drug.

                    [DatePublished] => 2014-06-28 00:00:00
                    [ColumnID] => 0
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                    [AuthorID] => 1804896
                    [AuthorName] => Sheila Crisostomo
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                    [ArticleID] => 1337206
                    [Title] => FDA bans medicine for blood clot
                    [Summary] => 
The Food and Drugs Administration (FDA) has temporarily banned the sale of a medicine used to treat blood clot from India due to reported serious adverse reactions to the drug.

                    [DatePublished] => 2014-06-21 00:00:00
                    [ColumnID] => 0
                    [Focus] => 0
                    [AuthorID] => 1097338
                    [AuthorName] =>  Mayen Jaymalin
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Dialysis drug reactions reach 130 cases

By Mayen Jaymalin | July 12, 2014 - 12:00am

At least 130 patients nationwide who have been undergoing dialysis experienced unusual chills due to a contaminated drug, the Food and Drug Administration (FDA) reported yesterday.

Metro

DOH to hospitals: Report adverse reactions to dialysis drug

By Sheila Crisostomo | June 28, 2014 - 12:00am

The Department of Health (DOH) urged all hospitals yesterday to report to the Food and Drug Administration (FDA) if they have patients who experienced adverse reactions to a dialysis drug.

Metro

FDA bans medicine for blood clot

By Mayen Jaymalin | June 21, 2014 - 12:00am

The Food and Drugs Administration (FDA) has temporarily banned the sale of a medicine used to treat blood clot from India due to reported serious adverse reactions to the drug.

Metro