Details for: MEDIPRO

Product description

Product name: MEDIPRO

DIN: 02231935

Status: Cancelled Post Market

Status date: 2009-08-18

Active ingredient(s)	Strength
ASCORBIC ACID (ASCORBIC ACID)	37.5 MG / 15 G
BIOTIN	75 MCG / 15 G
CALCIUM (CALCIUM CITRATE)	125 MG / 15 G
CHOLINE CITRATE	10 MG / 15 G
CHROMIUM (CHROMIUM CITRATE)	25 MCG / 15 G
COPPER (COPPER CITRATE)	1 MG / 15 G
D-PANTOTHENIC ACID	10 MG / 15 G
FOLIC ACID	0.07 MG / 15 G
IODINE (POTASSIUM IODIDE)	0.2 MG / 15 G
IRON (FERRIC CITRATE)	4 MG / 15 G
MAGNESIUM (MAGNESIUM CITRATE)	50 MG / 15 G
MANGANESE (MANGANESE CITRATE)	2.5 MG / 15 G
MOLYBDENUM (MOLYBDENUM CITRATE)	12.5 MCG / 15 G
NICOTINIC ACID	7.5 MG / 15 G
POTASSIUM (POTASSIUM CITRATE)	49 MG / 15 G
SELENIUM (SELENIUM CITRATE)	25 MCG / 15 G
VANADIUM (VANADIUM CITRATE)	12.5 MCG / 15 G
VITAMIN A (BETA-CAROTENE)	2000 UNIT / 15 G
VITAMIN B12 (VITAMIN B12)	15 MCG / 15 G
VITAMIN B1 (THIAMINE HYDROCHLORIDE)	2.5 MG / 15 G
VITAMIN B2 (RIBOFLAVIN-5-PHOSPHATE)	1 MG / 15 G
VITAMIN B6 (PYRIDOXAL-5-PHOSPHATE)	2.5 MG / 15 G
VITAMIN E (D-ALPHA TOCOPHEROL)	25 UNIT / 15 G
ZINC (ZINC CITRATE)	2.5 MG / 15 G

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For consumers

Resource	Description
Report a side effect	Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are: Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death; Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.

For health care professionals

Resource	Description
Report a serious adverse drug reaction (for hospitals)	Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to Health Canada all serious adverse drug reactions (ADRs) and medical device incidents (MDIs) within 30 days of being documented within the hospital. This regulatory requirement only applies to hospitals.

For researchers

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.

All resources

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.
Report a side effect	Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are: Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death; Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.
Report a serious adverse drug reaction (for hospitals)	Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to Health Canada all serious adverse drug reactions (ADRs) and medical device incidents (MDIs) within 30 days of being documented within the hospital. This regulatory requirement only applies to hospitals.

Resource	Description
Report a side effect	Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are: Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death; Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.

Resource	Description
Search Clinical Information	After Health Canada completes the regulatory review process for a product, the clinical information included in a submission is made publicly available for non-commercial purposes.
Report a side effect	Side effects are troublesome symptoms or feelings that you may not expect that show up when you are taking a medicine. All suspected side effects should be reported, especially those that are: Unexpected, regardless of their severity, i.e., not consistent with product information or labelling; or Serious, whether expected or not, i.e., that requires being admitted to the hospital, lengthened hospital stay, causes a birth defect, disability, is life-threatening or results in death; Reactions to recently marketed health products (on the market for less than five years), regardless of their nature or severity.
Report a serious adverse drug reaction (for hospitals)	Section C.01.020.1 of the Food and Drug Regulations and section 62 of the Medical Devices Regulations, require hospitals to report to Health Canada all serious adverse drug reactions (ADRs) and medical device incidents (MDIs) within 30 days of being documented within the hospital. This regulatory requirement only applies to hospitals.