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Advanced Side Effects

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Common Advanced Side Effects


The most commonly reported Advanced side effects (click to view or check a box to report):

Application Site Burn (4)
Accidental Exposure (2)
Ocular Hyperaemia (2)
Off Label Use (2)
Dyspnoea (2)
Burning Sensation (2)
Somnolence (1)
Application Site Hypersensitivity (1)
Chest Pain (1)
Eye Pain (1)
Chemical Burns Of Eye (1)
Eye Irritation (1)
Condition Aggravated (1)
Anaemia (1)
Application Site Urticaria (1)
Application Site Pruritus (1)
Application Site Erythema (1)
Application Site Vesicles (1)
Blood Amylase Increased (1)
Blood Pressure Decreased (1)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Advanced Side Effects Reported to FDA



Advanced Side Effect Report#8334424-7
Dry Eye, Skin Injury
This is a report of a 64-year-old female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: NA, who was treated with Advanced Eye Relief/dry Eye/environmental Lubricant Eye Drops (dosage: NA, start time:
Aug 10, 2011), combined with:
  • Propylene Glycol
  • Lotemax
  • Lotemax
  • Lotemax
  • Genteal
and developed a serious reaction and side effect(s): Dry Eye, Skin Injury after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Advanced Eye Relief/dry Eye/environmental Lubricant Eye Drops treatment in female patients, resulting in Dry Eye side effect.
Advanced Side Effect Report#8325667-7
Erythema, Dyspnoea, Urticaria, Dermatitis Contact, Rash Macular, Pruritus
This report suggests a potential Advanced Protection Spf 20 Erythema side effect(s) that can have serious consequences. A 48-year-old female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: therapeutic skin care topical and used Advanced Protection Spf 20 (dosage: NA) starting
Apr 25, 2012. After starting Advanced Protection Spf 20 the patient began experiencing various side effects, including: Erythema, Dyspnoea, Urticaria, Dermatitis Contact, Rash Macular, PruritusAdditional drugs used concurrently: NA.The patient was hospitalized. Although Advanced Protection Spf 20 demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Erythema, may still occur.
Advanced Side Effect Report#7383550-8
Application Site Pruritus, Application Site Erythema, Application Site Urticaria
This Application Site Pruritus problem was reported by a consumer or non-health professional from United States. A 59-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: skin wrinkling. On NS this consumer started treatment with Advanced Revitalift Deepset L'oreal Paris (dosage: Approx 1/2 Or 2 Ml Sample Pkge Once Top). The following drugs were being taken at the same time: NA. When using Advanced Revitalift Deepset L'oreal Paris, the patient experienced the following unwanted symptoms/side effects: Application Site Pruritus, Application Site Erythema, Application Site UrticariaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Application Site Pruritus, may become evident only after a product is in use by the general population.
Advanced Side Effect Report#7298350-7
Hypertension, Anaemia, Hypophosphataemia, Hypothyroidism, Hot Flush, Blood Amylase Increased, Delirium, Hepatic Function Abnormal, White Blood Cell Count Decreased
This Hypertension side effect was reported by a physician from Japan. A female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Advanced Renal Cell Carcinoma, Sorafenib 400mg (drug dosage: 400 Mg, Unk), which was initiated on
Sep 17, 2009. Concurrently used drugs:
  • Cefmetazon (2 G, Unk)
  • Fresmin (2 Mg, Unk)
.After starting to take Advanced Renal Cell Carcinoma, Sorafenib 400mg the consumer reported adverse symptoms, such as: Hypertension, Anaemia, Hypophosphataemia, Hypothyroidism, Hot Flush, Blood Amylase Increased, Delirium, Hepatic Function Abnormal, White Blood Cell Count DecreasedThese side effects may potentially be related to Advanced Renal Cell Carcinoma, Sorafenib 400mg.
Advanced Side Effect Report#7229826-6
Impaired Driving Ability, Off Label Use, Intentional Overdose
This is a report of a 49-year-old female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: alcohol use, who was treated with Advanced Listerine With Tartar Protection (dosage: Text:drank About Half A Bottle, Half Of 8.5oz, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Impaired Driving Ability, Off Label Use, Intentional Overdose after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Advanced Listerine With Tartar Protection treatment in female patients, resulting in Impaired Driving Ability side effect.
Advanced Side Effect Report#7102886-9
Application Site Hypersensitivity, Condition Aggravated, Skin Wrinkling
This report suggests a potential Advanced Firming + Anti Wrinkle Moisture Night Cream Application Site Hypersensitivity side effect(s) that can have serious consequences. A 37-year-old female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: skin wrinkling and used Advanced Firming + Anti Wrinkle Moisture Night Cream (dosage: Application, Topical, Single) starting
Oct 23, 2010. After starting Advanced Firming + Anti Wrinkle Moisture Night Cream the patient began experiencing various side effects, including: Application Site Hypersensitivity, Condition Aggravated, Skin WrinklingAdditional drugs used concurrently: NA. Although Advanced Firming + Anti Wrinkle Moisture Night Cream demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Application Site Hypersensitivity, may still occur.
Advanced Side Effect Report#7094585-7
Dizziness, Hallucination, Visual, Nausea
This Dizziness problem was reported by a consumer or non-health professional from United States. A 16-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: alcohol use. On
Oct 03, 2010 this consumer started treatment with Advanced Listerine With Tartar Protection (dosage: Text:entire Bottle). The following drugs were being taken at the same time: NA. When using Advanced Listerine With Tartar Protection, the patient experienced the following unwanted symptoms/side effects: Dizziness, Hallucination, Visual, NauseaThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Dizziness, may become evident only after a product is in use by the general population.
Advanced Side Effect Report#6470449-4
Chest Discomfort, Dysgeusia, Off Label Use, Palpitations, Paraesthesia
This Chest Discomfort side effect was reported by a consumer or non-health professional from United States. A 57-year-old male patient (weight:NA) experienced the following symptoms/conditions: stomatitis,epilepsy.The patient was prescribed Advanced Listerine With Tartar Protection (drug dosage: Text:a Mouthful Once), which was initiated on
Nov 22, 2009. Concurrently used drugs:
  • Carbamazepine
  • Clonazepam
  • Afrin
.After starting to take Advanced Listerine With Tartar Protection the consumer reported adverse symptoms, such as: Chest Discomfort, Dysgeusia, Off Label Use, Palpitations, ParaesthesiaThese side effects may potentially be related to Advanced Listerine With Tartar Protection.
Advanced Side Effect Report#6441991-7
Accidental Exposure, Emotional Distress, Oesophageal Spasm, Oropharyngeal Pain, Pharyngeal Erythema, Product Quality Issue
This is a report of a female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: dental disorder prophylaxis,hypertension, who was treated with Advanced Listerine With Tartar Protection (dosage: NA, start time: NS), combined with:
  • Cozaar
  • Atenolol
  • Diuretics
and developed a serious reaction and side effect(s): Accidental Exposure, Emotional Distress, Oesophageal Spasm, Oropharyngeal Pain, Pharyngeal Erythema, Product Quality Issue after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Advanced Listerine With Tartar Protection treatment in female patients, resulting in Accidental Exposure side effect.
Advanced Side Effect Report#6110639-3
Application Site Burn, Application Site Vesicles, Oral Disorder
This report suggests a potential Advanced Listerine With Tartar Protection Application Site Burn side effect(s) that can have serious consequences. A 21-year-old male patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: dental disorder prophylaxis and used Advanced Listerine With Tartar Protection (dosage: Text:20 Ml Once Per Day) starting NS. After starting Advanced Listerine With Tartar Protection the patient began experiencing various side effects, including: Application Site Burn, Application Site Vesicles, Oral DisorderAdditional drugs used concurrently: NA. Although Advanced Listerine With Tartar Protection demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Application Site Burn, may still occur.
Advanced Side Effect Report#6036131-2
Application Site Burn, Rosacea, Swelling Face
This Application Site Burn problem was reported by a consumer or non-health professional from United States. A 88-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: dental disorder prophylaxis. On NS this consumer started treatment with Advanced Listerine Mouthwash Citrus (dosage: NA). The following drugs were being taken at the same time:
  • Diovan (Text:360 Mg)
  • Synthroid (Text:125 Mg)
When using Advanced Listerine Mouthwash Citrus, the patient experienced the following unwanted symptoms/side effects: Application Site Burn, Rosacea, Swelling FaceAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Application Site Burn, may become evident only after a product is in use by the general population.
Advanced Side Effect Report#5977861-8
Application Site Burn
This Application Site Burn side effect was reported by a consumer or non-health professional from United States. A 43-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Advanced Listerine Mouthwash Citrus (drug dosage: Text:half Capful Once), which was initiated on
Nov 22, 2008. Concurrently used drugs:
  • Atenolol (Text:12.5 Mg Twice Daily)
.After starting to take Advanced Listerine Mouthwash Citrus the consumer reported adverse symptoms, such as: Application Site BurnThese side effects may potentially be related to Advanced Listerine Mouthwash Citrus.
Advanced Side Effect Report#5884181-9
Application Site Burn
This is a report of a 64-year-old female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: dry eye, who was treated with Advanced Relief Visine (dosage: Text:^couple^ Once, start time:
Sep 04, 2008), combined with: NA. and developed a serious reaction and side effect(s): Application Site Burn after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Advanced Relief Visine treatment in female patients, resulting in Application Site Burn side effect.
Advanced Side Effect Report#5751530-1
Eye Irritation, Irritability, Ocular Hyperaemia, Visual Disturbance
This report suggests a potential Advanced Relief Visine (povidone, Dextran 70, Polyethylene Glycol, Tet Eye Irritation side effect(s) that can have serious consequences. A 77-year-old female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: dry eye and used Advanced Relief Visine (povidone, Dextran 70, Polyethylene Glycol, Tet (dosage: One Drop In Each Eye, Once, Ophthalmic) starting
Nov 22, 2007. After starting Advanced Relief Visine (povidone, Dextran 70, Polyethylene Glycol, Tet the patient began experiencing various side effects, including: Eye Irritation, Irritability, Ocular Hyperaemia, Visual DisturbanceAdditional drugs used concurrently: NA. Although Advanced Relief Visine (povidone, Dextran 70, Polyethylene Glycol, Tet demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Eye Irritation, may still occur.
Advanced Side Effect Report#5748511-0
Malaise
This Malaise problem was reported by a consumer or non-health professional from United States. A 30-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Feb 01, 2008 this consumer started treatment with Advanced Listerine With Tartar Protection (menthol, Methyl Salicylate, (dosage: Whole Bottles At A Time Once A Day, Oral). The following drugs were being taken at the same time: NA. When using Advanced Listerine With Tartar Protection (menthol, Methyl Salicylate,, the patient experienced the following unwanted symptoms/side effects: MalaiseAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Malaise, may become evident only after a product is in use by the general population.
Advanced Side Effect Report#5678308-1
Burning Sensation, Oral Discomfort
This Burning Sensation side effect was reported by a consumer or non-health professional from United States. A 80-year-old female patient (weight:NA) experienced the following symptoms/conditions: dental disorder prophylaxis.The patient was prescribed Advanced Listerine With Tartar Protection (menthol, Methyl Salicylate, (drug dosage: NA), which was initiated on
Jan 04, 2008. Concurrently used drugs:
  • Diovan
  • Avandia
  • Antidepressants (antidepressants)
  • Synthroid
.After starting to take Advanced Listerine With Tartar Protection (menthol, Methyl Salicylate, the consumer reported adverse symptoms, such as: Burning Sensation, Oral DiscomfortThese side effects may potentially be related to Advanced Listerine With Tartar Protection (menthol, Methyl Salicylate,.
Advanced Side Effect Report#5643933-0
Accidental Exposure, Burning Sensation, Chest Pain, Dyspnoea
This is a report of a 75-year-old male patient (weight: NA) from United States, suffering from the following health symptoms/conditions: dental disorder prophylaxis, who was treated with Advanced Listerine With Tartar Protection (menthol, Methyl Salicylate, (dosage: 20 Ml, 2 Times A Day, Oral, start time:
Jan 19, 2008), combined with:
  • Atenolol
  • Aspirin
  • Altace
  • Protonix
  • Vytorin
and developed a serious reaction and side effect(s): Accidental Exposure, Burning Sensation, Chest Pain, Dyspnoea after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Advanced Listerine With Tartar Protection (menthol, Methyl Salicylate, treatment in male patients, resulting in Accidental Exposure side effect. The patient was hospitalized.
Advanced Side Effect Report#5342014-3
Menstruation Irregular, Stress, Weight Increased
This report suggests a potential Advanced Woman's Formula Multivitamins Futurebiotics Menstruation Irregular side effect(s) that can have serious consequences. A 24-year-old female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: fatigue,iron deficiency and used Advanced Woman's Formula Multivitamins Futurebiotics (dosage: 2 Tablets Daily) starting
Sep 01, 2006. After starting Advanced Woman's Formula Multivitamins Futurebiotics the patient began experiencing various side effects, including: Menstruation Irregular, Stress, Weight IncreasedAdditional drugs used concurrently: NA. Although Advanced Woman's Formula Multivitamins Futurebiotics demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Menstruation Irregular, may still occur.
Advanced Side Effect Report#5026763-2
Chemical Burns Of Eye, Eye Discharge, Eye Pain, Eye Swelling, Ocular Hyperaemia, Superficial Injury Of Eye
This Chemical Burns Of Eye problem was reported by a consumer or non-health professional from United States. A 18-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: eye irritation. On
May 29, 2006 this consumer started treatment with Advanced Relief Visine (povidone, Dextran 70, Polyethylene Glycol, Tet (dosage: 1-2 Drops Once In Left Eye, Ophthalmic). The following drugs were being taken at the same time: NA. When using Advanced Relief Visine (povidone, Dextran 70, Polyethylene Glycol, Tet, the patient experienced the following unwanted symptoms/side effects: Chemical Burns Of Eye, Eye Discharge, Eye Pain, Eye Swelling, Ocular Hyperaemia, Superficial Injury Of EyeAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Chemical Burns Of Eye, may become evident only after a product is in use by the general population.
Advanced Side Effect Report#4840135-2
Blood Pressure Decreased, Lethargy, Somnolence
This Blood Pressure Decreased side effect was reported by a consumer or non-health professional from United States. A male patient (weight:NA) experienced the following symptoms/conditions: accidental exposure.The patient was prescribed Advanced Relief Visine (povidone, Dextran 70, Polyethylene Glycol, Tet (drug dosage: Oral), which was initiated on
Nov 14, 2005. Concurrently used drugs: NA..After starting to take Advanced Relief Visine (povidone, Dextran 70, Polyethylene Glycol, Tet the consumer reported adverse symptoms, such as: Blood Pressure Decreased, Lethargy, SomnolenceThese side effects may potentially be related to Advanced Relief Visine (povidone, Dextran 70, Polyethylene Glycol, Tet. The patient was hospitalized.



The appearance of Advanced on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    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.

    Advanced reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    Advanced Safety Alerts, Active Ingredients, Usage Information

    NDC0023-4307
    TypeHUMAN OTC DRUG
    Proprietary NameREFRESH OPTIVE Advanced carboxymethylcellulose sodium, glycerin, and polysorbate 80
    NameSOLUTION/ DROPS
    Dosage FormOPHTHALMIC
    Route20111130
    On market sinceAllergan, Inc.
    LabelerCARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN; POLYSORBATE 80
    Active Ingredient(s)5; 10; 5
    Strength(s)mg/mL; mg/mL; mg/mL
    Unit(s)
    Pharma Class

    More About Advanced

    Side Effects reported to FDA: 20

    Advanced safety alerts: 2014 2013 2012 2007 2006

    Reported deaths: 1

    Reported hospitalizations: 1

    Maxiloss Weight Advanced Softgels: Recall - Undeclared Drug Ingredient

     

    [Posted 02/25/2013]

    AUDIENCE: Consumer

    ISSUE: Olaax Corp announced a nationwide recall of the company's dietary supplement sold under the brand name Maxiloss Weight Advanced Softgels to the user level, because FDA testing found the Maxiloss Weight Advanced product to contain Sibutramine. Sibutramine was a previously approved controlled substance for the treatment of obesity that was removed from the U.S. market in October 2010 for safety reasons, making this product an unapproved new drug.

    Sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk to patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. Sibutramine has been withdrawn from U.S marketplace. The active drug ingredient is not listed on the label for these products.

    The recall includes ALL authentic lot numbers and known to be counterfeit lot numbers of authentic lots. Any packaging types that are different from listed are counterfeit. Any lot numbers not listed are counterfeit and are also part of the recall.

    BACKGROUND: Maxiloss Weight Advanced Softgels is marketed as a Natural Herb for Weight Loss. The product is packaged in a green or blue box containing 3 X 12 blister packs per box and bears "Batch Number: 001". The product was sold to distributors nationwide, and known-to-be counterfeit versions are sold on various online sites. This product was distributed nationwide in US from January 2011 to November 2012.

    RECOMMENDATION: Consumers with questions regarding this recall can contact Olaax Corporation at 1-863-648-9581, Monday through Friday, 9:00 am to 5:30 pm, EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking this drug product.


    [02/25/2013 - Press Release - Olaax Corp]

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