Multivitamin Side Effects
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View and Submit Multivitamin Side Effects
Your Multivitamin Side Effect submission can play a very important role. Reporting your experience could help identify an unknown risk and inform other patients and health care professionals.
Record and Track Your Side Effects
It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.
Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Active Ingredient: .ALPHA.-T AVOBENZON
Side Effects reported to FDA: 355. View Multivitamin Adverse Reports
Multivitamin safety alerts: 2013
Reported deaths: 6
Reported hospitalizations: 51
Eba Multivitamin Supplement By Saratoga Therapeutics LLC: Recall - Allergy Alert On Undeclared Milk Components
AUDIENCE: Consumer, Patient, Health Professional
ISSUE: Saratoga Therapeutics, LLC of North Wales, PA recalled 900 bottles of ebA Multivitamin Supplement because they may contain undeclared milk components – milk protein(s) and lactose. The label lists the product as being free of milk components. People with an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction and people who have lactose intolerance run the risk of gastrointestinal symptoms if they consume ebA Multivitamin Supplement.
Affected lot numbers include #0912164 expiration date 12/12 and #1110354 expiration date 10/14.
BACKGROUND: ebA Multivitamin Supplement was distributed nationwide and in Australia, Canada, Costa Rica, England, Finland, Ireland, Malaysia, Switzerland, and Tasmania. and reached consumers by mail order, fax order, internet sales and doctors' office sales. The vitamins are packaged in a white plastic bottle with white, green and blue labeling. The expiration date is listed beneath the Warning section on the label.
RECOMMENDATION: Consumers who have purchased ebA Multivitamin Supplement may return any unused portion of the product to Saratoga Therapeutics, LLC for a refund. Contact the company at info@ebAMultivitamin.com or 215-661-9044 8:30 a.m. to 4:30 p.m. east coast time to request mailing materials and/or for any questions.
Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:
[04/23/2013 - Press Release - Saratoga Therapeutics]
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Multivitamin Adverse Reactions
Headache ( 22 Reports)|Fatigue ( 20 Reports)|Pain ( 19 Reports)|Dizziness ( 18 Reports)|Nausea ( 18 Reports)|Insomnia ( 16 Reports)|Dyspnoea ( 15 Reports)|Pruritus ( 14 Reports)|Rash ( 14 Reports)|Diarrhoea ( 13 Reports)|Convulsion ( 12 Reports)|Depression ( 12 Reports)|Injection Site Pain ( 12 Reports)|Paraesthesia ( 11 Reports)|Vomiting ( 11 Reports)|Arthralgia ( 10 Reports)|Constipation ( 10 Reports)|Cough ( 10 Reports)|Asthenia ( 9 Reports)|Product Quality Issue ( 9 Reports)|Malaise ( 8 Reports)|Pyrexia ( 8 Reports)|Urinary Tract Infection ( 8 Reports)|Anxiety ( 7 Reports)|Blood Glucose Increased ( 7 Reports)|Chest Pain ( 7 Reports)|Feeling Abnormal ( 7 Reports)|Feeling Hot ( 7 Reports)|Flushing ( 7 Reports)|Muscle Spasms ( 7 Reports)|