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Allergy (19)
Dizziness (13)
HEADACHES (12)
Bowl Movements With Oder (11)
Excessive Gas (7)
Terribel Leg Cramps (6)
Ankle Swelling (6)
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Ocuvite Side Effects and Adverse Effects reported to US Food and Drug Administration (FDA)

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Swelling Face, Dyspnoea, Pulmonary Oedema (8469660-2)
on Jun 21, 2012 Female from CANADA , 76 years of age, weighting 138.9 lb, was treated with Ocuvite Plus With Lutein. Directly after, patient experienced the unwanted or unexpected Ocuvite side effects: swelling face, dyspnoea, pulmonary oedema. Ocuvite Plus With Lutein dosage: N/A.
Associated medications used:
  • Hydroxychloroquine Sulfate
  • Leflunomide
  • Humira
  • Celebrex
  • Sulfasalazine
  • Afi-b-total
  • Vitalux
Patient was hospitalized.

Pulmonary Embolism (8453815-7)
Patient was taking Ocuvite (ocuvite). Patient felt the following Ocuvite side effects: pulmonary embolism on Nov 01, 2011 from UNITED STATES Additional patient health information: Female , 80 years of age, . Ocuvite (ocuvite) dosage: N/A.
Multiple prescriptions taken:
  • 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)
Patient was hospitalized.

Prothrombin Time Prolonged (8369102-1)
Adverse event was reported on May 16, 2012 by a Male taking Ocuvite With Lutein Bausch+lomb (Dosage: 1 Tablet Daily Po) was diagnosed with
  • eye haemorrhage
  • cardiac valve disease
and. Location: UNITED STATES , 76 years of age, weighting 170.0 lb, After Ocuvite was administered, patient encountered several Ocuvite side effects: prothrombin time prolonged.

Ecchymosis (7640247-4)
on Jun 27, 2011 Female from UNITED STATES , 82 years of age, weighting 130.1 lb, was treated with Ocuvite [vit C,betacarot,cupric Oxide,se+,vit E,zno]. Directly after, patient experienced the unwanted or unexpected Ocuvite side effects: ecchymosis. Ocuvite [vit C,betacarot,cupric Oxide,se+,vit E,zno] dosage: N/A.
Associated medications used:
  • Glucosamine
  • Aleve (caplet) (220 Mg, Prn)
  • Citracal
  • Multi-vitamins
  • Synthroid
  • Pravastatin



Choking Sensation, Dysphagia, Dyspnoea, Foreign Body Trauma, Oropharyngeal Pain (5808767-2)
on Jul 10, 2008 Female from UNITED STATES , 71 years of age, weighting 155.0 lb, was diagnosed with
  • eye disorder
and was treated with Ocuvite Adult Soft Gel Bausch + Lomb. Patient felt the following Ocuvite side effects: choking sensation, dysphagia, dyspnoea, foreign body trauma, oropharyngeal pain. Ocuvite Adult Soft Gel Bausch + Lomb dosage: 1 Soft Gel Green Capsule 1 Po.

Abdominal Pain, Diarrhoea, Faeces Discoloured (5642934-6)
Patient was taking Ocuvite Adult 50+ 50+ Bausch And Lomb. After Ocuvite was administered, patient encountered several Ocuvite side effects: abdominal pain, diarrhoea, faeces discoloured on Feb 27, 2008 from UNITED STATES Additional patient health information: Female , 86 years of age, weighting 140.0 lb, . Ocuvite Adult 50+ 50+ Bausch And Lomb dosage: 1 Capsule Daily Po.

Accidental Overdose, Anxiety, Atrial Fibrillation, Cardiac Flutter, Contusion, Diarrhoea, Fatigue, Heart Rate Increased, Injection Site Bruising (5164645-6)
Adverse event was reported on Feb 17, 2006 by a Female taking Ocuvite (Dosage: N/A) . Location: UNITED STATES , 78 years of age, Directly after, patient experienced the unwanted or unexpected Ocuvite side effects: accidental overdose, anxiety, atrial fibrillation, cardiac flutter, contusion, diarrhoea, fatigue, heart rate increased, injection site bruising.
Associated medications used:
  • Forteo
  • Forteo (Unk, Unk)
  • Femara
  • Tylenol
  • Calcium
Patient was hospitalized.

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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.

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