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Ocuvite Side Effects

Common Ocuvite Side Effects


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

Diarrhoea (2)
Dyspnoea (2)
Pulmonary Embolism (1)
Prothrombin Time Prolonged (1)
Pulmonary Oedema (1)
Oropharyngeal Pain (1)
Injection Site Bruising (1)
Fatigue (1)
Foreign Body Trauma (1)
Heart Rate Increased (1)
Faeces Discoloured (1)
Dysphagia (1)
Cardiac Flutter (1)
Choking Sensation (1)
Contusion (1)
Atrial Fibrillation (1)
Anxiety (1)
Abdominal Pain (1)
Accidental Overdose (1)
Ecchymosis (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.

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.

Ocuvite Side Effects Reported to FDA

The following Ocuvite 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.


The appearance of Ocuvite 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.
Swelling Face, Dyspnoea, Pulmonary Oedema
This is a report of a 76-year-old female patient (weight: NA) from CANADA, suffering from the following symptoms/conditions: NA, who was treated with Ocuvite Plus With Lutein (dosage: NA, start time: NS), combined with:
  • Hydroxychloroquine Sulfate
  • Leflunomide
  • Humira
  • Celebrex
  • Sulfasalazine
  • Afi-b-total
  • Vitalux
and developed a serious reaction and side effect(s). The consumer presented with:
  • Swelling Face
  • Dyspnoea
  • Pulmonary Oedema
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Ocuvite Plus With Lutein treatment in female patients, resulting in swelling face side effect. The patient was hospitalized.

Pulmonary Embolism
This report suggests a potential Ocuvite (ocuvite) Pulmonary Embolism side effect(s) that can have serious consequences. A 80-year-old female patient (weight: NA) from UNITED STATES was diagnosed with the following symptoms/conditions: NA and used Ocuvite (ocuvite) (dosage: NA) starting Feb 13, 2009. Soon after starting Ocuvite (ocuvite) the patient began experiencing various side effects, including:
  • Pulmonary Embolism
Drugs used concurrently:
  • Centrum (centrum)
  • Glucosamide-chondroitin (glucosamide W/chondroitin Sulfate)
  • Morphine Sulfate Inj
  • Calcium Carbonate
  • Tylenol Arthritis Pain (paracetamol)
  • Revlimid (10 Mg, Daily X 21 Days, Po)
The patient was hospitalized. Although Ocuvite (ocuvite) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as pulmonary embolism, may still occur.

Prothrombin Time Prolonged
This Prothrombin Time Prolonged problem was reported by a physician from UNITED STATES. A 76-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: eye haemorrhage,cardiac valve disease. On NS this consumer started treatment with Ocuvite With Lutein Bausch+lomb (dosage: 1 Tablet Daily Po). The following drugs were being taken at the same time: NA. When commencing Ocuvite With Lutein Bausch+lomb, the patient experienced the following unwanted symptoms/side effects:
  • Prothrombin Time Prolonged
Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as prothrombin time prolonged, may become evident only after a product is in use by the general population.

Ecchymosis
This is a report of a 82-year-old female patient (weight: NA) from UNITED STATES. The patient developed the following symptoms/conditions: NA and was treated with Ocuvite [vit C,betacarot,cupric Oxide,se+,vit E,zno] (dosage: NA) starting Jun 20, 2011. Concurrently used drugs:
  • Glucosamine
  • Aleve (caplet) (220 Mg, Prn)
  • Citracal
  • Multi-vitamins
  • Synthroid
  • Pravastatin
Soon after that, the consumer experienced the following side effects:
  • Ecchymosis
This opens a possibility that Ocuvite [vit C,betacarot,cupric Oxide,se+,vit E,zno] treatment could cause the above reactions, including ecchymosis, and some female subjects may be more susceptible.


Choking Sensation, Dysphagia, Dyspnoea, Foreign Body Trauma, Oropharyngeal Pain
A 71-year-old female patient (weight: NA) from UNITED STATES with the following symptoms/conditions: eye disorder started Ocuvite Adult Soft Gel Bausch + Lomb treatment (dosage: 1 Soft Gel Green Capsule 1 Po) on NS. Soon after starting Ocuvite Adult Soft Gel Bausch + Lomb treatment, the subject experienced various side effects, including:
  • Choking Sensation
  • Dysphagia
  • Dyspnoea
  • Foreign Body Trauma
  • Oropharyngeal Pain
Concurrently used drugs: NA. This finding indicates that some female patients could be more vulnerable to Ocuvite Adult Soft Gel Bausch + Lomb.

Abdominal Pain, Diarrhoea, Faeces Discoloured
A 86-year-old female patient from UNITED STATES (weight: NA) experienced symptoms, such as: NA and was treated with Ocuvite Adult 50+ 50+ Bausch And Lomb(dosage: 1 Capsule Daily Po). The treatment was initiated on Feb 01, 2008. After that a consumer reported the following side effect(s):
  • Abdominal Pain
  • Diarrhoea
  • Faeces Discoloured
Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Ocuvite Adult 50+ 50+ Bausch And Lomb efficacy: NA.

Accidental Overdose, Anxiety, Atrial Fibrillation, Cardiac Flutter, Contusion, Diarrhoea, Fatigue, Heart Rate Increased, Injection Site Bruising
In this report, Ocuvite was administered for the following condition: NA.A 78-year-old female consumer from UNITED STATES (weight: NA) started Ocuvite treatment (dosage: NA) on Feb 15, 2006.Sometime after starting the treatment, the patient complained of the following side effect(s):
  • Accidental Overdose
  • Anxiety
  • Atrial Fibrillation
  • Cardiac Flutter
  • Contusion
  • Diarrhoea
  • Fatigue
  • Heart Rate Increased
  • Injection Site Bruising
A possible interaction with other drugs could have contributed to this reaction:
  • Forteo
  • Forteo (Unk, Unk)
  • Femara
  • Tylenol
  • Calcium
The patient was hospitalized.Establishing a causal relationship between a specific drug and consumer's side effects is complex, but it is possible that in this report Ocuvite treatment could be related to the listed above side effect(s).



Top 10 Ocuvite Side Effects for Women

Women Side EffectsReports
Diarrhoea 2
Dyspnoea 2
Abdominal Pain 1
Accidental Overdose 1
Anxiety 1
Atrial Fibrillation 1
Cardiac Flutter 1
Choking Sensation 1
Contusion 1
Dysphagia 1

Top 10 Ocuvite Side Effects for Men

Men Side EffectsReports
Prothrombin Time Prolonged 1

Keep Track of Side Effects

Note Your Observations

It is really important to keep of your 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

    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.


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    Ocuvite Safety Alerts, Active Ingredients, Usage Information

    More About Ocuvite

    Side Effects reported to FDA: 7

    Ocuvite safety alerts: No

    Reported hospitalizations: 2

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