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Ocuvite Side Effects

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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.

Ocuvite Side Effects Reported to FDA



Ocuvite Side Effect Report#8469660-2
Swelling Face, Dyspnoea, Pulmonary Oedema
This is a report of a 76-year-old female patient (weight: NA) from Canada, suffering from the following health 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): Swelling Face, Dyspnoea, Pulmonary Oedema 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.
Ocuvite Side Effect Report#8453815-7
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. After starting Ocuvite (ocuvite) the patient began experiencing various side effects, including: Pulmonary EmbolismAdditional 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.
Ocuvite Side Effect Report#8369102-1
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 using Ocuvite With Lutein Bausch+lomb, the patient experienced the following unwanted symptoms/side effects: Prothrombin Time ProlongedAlthough 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.
Ocuvite Side Effect Report#7640247-4
Ecchymosis
This Ecchymosis side effect was reported by a consumer or non-health professional from United States. A 82-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Ocuvite [vit C,betacarot,cupric Oxide,se+,vit E,zno] (drug dosage: NA), which was initiated on
Jun 20, 2011. Concurrently used drugs:
  • Glucosamine
  • Aleve (caplet) (220 Mg, Prn)
  • Citracal
  • Multi-vitamins
  • Synthroid
  • Pravastatin
.After starting to take Ocuvite [vit C,betacarot,cupric Oxide,se+,vit E,zno] the consumer reported adverse symptoms, such as: EcchymosisThese side effects may potentially be related to Ocuvite [vit C,betacarot,cupric Oxide,se+,vit E,zno].
Ocuvite Side Effect Report#5808767-2
Choking Sensation, Dysphagia, Dyspnoea, Foreign Body Trauma, Oropharyngeal Pain
This is a report of a 71-year-old female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: eye disorder, who was treated with Ocuvite Adult Soft Gel Bausch + Lomb (dosage: 1 Soft Gel Green Capsule 1 Po, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Choking Sensation, Dysphagia, Dyspnoea, Foreign Body Trauma, Oropharyngeal Pain after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Ocuvite Adult Soft Gel Bausch + Lomb treatment in female patients, resulting in Choking Sensation side effect.
Ocuvite Side Effect Report#5642934-6
Abdominal Pain, Diarrhoea, Faeces Discoloured
This report suggests a potential Ocuvite Adult 50+ 50+ Bausch And Lomb Abdominal Pain side effect(s) that can have serious consequences. A 86-year-old female patient (weight: NA) from United States was diagnosed with the following symptoms/conditions: NA and used Ocuvite Adult 50+ 50+ Bausch And Lomb (dosage: 1 Capsule Daily Po) starting
Feb 01, 2008. After starting Ocuvite Adult 50+ 50+ Bausch And Lomb the patient began experiencing various side effects, including: Abdominal Pain, Diarrhoea, Faeces DiscolouredAdditional drugs used concurrently: NA. Although Ocuvite Adult 50+ 50+ Bausch And Lomb demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Abdominal Pain, may still occur.
Ocuvite Side Effect Report#5164645-6
Accidental Overdose, Anxiety, Atrial Fibrillation, Cardiac Flutter, Contusion, Diarrhoea, Fatigue, Heart Rate Increased, Injection Site Bruising
This Accidental Overdose problem was reported by a consumer or non-health professional from United States. A 78-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Feb 15, 2006 this consumer started treatment with Ocuvite (dosage: NA). The following drugs were being taken at the same time:
  • Forteo
  • Forteo (Unk, Unk)
  • Femara
  • Tylenol
  • Calcium
When using Ocuvite, the patient experienced the following unwanted symptoms/side effects: Accidental Overdose, Anxiety, Atrial Fibrillation, Cardiac Flutter, Contusion, Diarrhoea, Fatigue, Heart Rate Increased, Injection Site BruisingThe 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 Accidental Overdose, may become evident only after a product is in use by the general population.



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.

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What are common 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

What are common Ocuvite Side Effects for Men?

Men Side EffectsReports
Prothrombin Time Prolonged 1

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.

    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.

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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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