ACULAR Side Effects

6929981-9 | Blood Pressure Systolic Increased, Cyst, Eye Disorder, Eye Inflammation, Eye Pain, Eye Swelling, Headache, Ocular Hyperaemia
on Aug 17, 2010 Female patient from UNITED STATES , 78 years of age, weighting 135.0 lb, was diagnosed with cyst, inflammation and was treated with Acular (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure systolic increased, cyst, eye disorder, eye inflammation, eye pain, eye swelling, headache (What is headache?), ocular hyperaemia. Acular dosage: One Drop 4 Times Daily. During the same period patient was treated with KETOROLAC TROMETHAMINE (One Drop 4 Times Daily) (View Ketorolac Tromethamine Review and Ketorolac Tromethamine Label ).

6790291-4 | Asthma
Patient was taking Acular (View Usage). Patient had the following side effects: asthma (What is asthma?) on Jun 16, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 43 years of age, was diagnosed with blepharitis and. Acular dosage: Unk.

6702904-3 | No Adverse Event
Adverse event was reported on Apr 29, 2010 by a Male patient taking Acular (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 200.0 lb, After Acular was administered, patient had the following side effects: no adverse event.

6615885-8 | Punctate Keratitis
on Feb 24, 2010 Female patient from SOUTH AFRICA , 78 years of age, was diagnosed with postoperative care, inflammation and was treated with Acular (View Usage). Patient experienced the following unwanted or unexpected effects: punctate keratitis. Acular dosage: Unk. During the same period patient was treated with EXOCIN (Unk) (View Exocin Review and Exocin Label ), PRED FORTE (Unk) (View Pred Forte Review and Pred Forte Label ), MAXITROL (Unk) (View Maxitrol Review and Maxitrol Label ).


6612888-4 | Keratitis
on Mar 01, 2010 Male patient from SOUTH AFRICA , 60 years of age, was treated with Acular (View Usage). Patient had the following side effects: keratitis. Acular dosage: Unk. During the same period patient was treated with EXOCIN (Unk) (View Exocin Review and Exocin Label ), PRED FORTE (Unk) (View Pred Forte Review and Pred Forte Label ), MAXITROL (Unk) (View Maxitrol Review and Maxitrol Label ).

6509387-7 | Ulcerative Keratitis, Visual Acuity Reduced
Patient was taking Acular (View Usage). After Acular was administered, patient had the following side effects: ulcerative keratitis, visual acuity reduced on Dec 17, 2009 from FRANCE Additional patient health information: Male patient , 75 years of age, was diagnosed with conjunctivitis and. Acular dosage: Unk. During the same period patient was treated with INDOBIOTIC (Unk) (View Indobiotic Review and Indobiotic Label ). Patient was hospitalized.

6410974-5 | Eye Inflammation, Eye Pain, Vision Blurred, Visual Acuity Reduced
Adverse event was reported on Oct 20, 2009 by a Female patient taking Acular (View Usage) (Dosage: 1 Drop B.i.d. R. Eye) was diagnosed with cataract operation and. Location: UNITED STATES , 76 years of age, weighting 92.00 lb, Patient experienced the following unwanted or unexpected effects: eye inflammation, eye pain, vision blurred, visual acuity reduced.

6334605-8 | Corneal Perforation, Ulcerative Keratitis
on Aug 24, 2009 Male patient from SOUTH AFRICA , 66 years of age, was diagnosed with cataract operation, postoperative care and was treated with Acular (View Usage). Patient had the following side effects: corneal perforation, ulcerative keratitis. Acular dosage: 1 Gtt, Qid. During the same period patient was treated with TOBRADEX (Unk) (View Tobradex Review and Tobradex Label ).

6332267-7 | Corneal Epithelium Defect, Corneal Thinning, Eye Pain, Iridocele, Ocular Hyperaemia, Ulcer, Visual Acuity Reduced
on Aug 24, 2009 Male patient from SOUTH AFRICA , 76 years of age, was treated with Acular (View Usage). After Acular was administered, patient had the following side effects: corneal epithelium defect, corneal thinning, eye pain, iridocele, ocular hyperaemia, ulcer (What is ulcer?), visual acuity reduced. Acular dosage: . During the same period patient was treated with PRED FORTE (View Pred Forte Review and Pred Forte Label ), ZYMAR (View Zymar Review and Zymar Label ).

6326856-3 | Corneal Epithelium Defect, Corneal Thinning, Eye Pain, Iridocele, Ocular Hyperaemia, Ulcer, Visual Acuity Reduced
Patient was taking Acular (View Usage). Patient experienced the following unwanted or unexpected effects: corneal epithelium defect, corneal thinning, eye pain, iridocele, ocular hyperaemia, ulcer (What is ulcer?), visual acuity reduced on Aug 19, 2009 from SOUTH AFRICA Additional patient health information: Male patient , 76 years of age, . Acular dosage: . During the same period patient was treated with PRED FORTE (View Pred Forte Review and Pred Forte Label ), ZYMAR (View Zymar Review and Zymar Label ).

6314048-3 | Corneal Epithelium Defect, Corneal Thinning, Eye Pain, Iridocele, Ocular Hyperaemia, Visual Acuity Reduced
Adverse event was reported on Aug 13, 2009 by a Male patient taking Acular (View Usage) (Dosage: ) . Location: , 76 years of age, Patient had the following side effects: corneal epithelium defect, corneal thinning, eye pain, iridocele, ocular hyperaemia, visual acuity reduced. During the same period patient was treated with PRED FORTE (View Pred Forte Review and Pred Forte Label ), ZYMAR (View Zymar Review and Zymar Label ).

6269886-2 | Ulcerative Keratitis
on Jul 10, 2009 Female patient from SPAIN , 70 years of age, was diagnosed with postoperative care, pain (What is pain?), erythema, lacrimation increased, blepharospasm, ciliary hyperaemia, corneal thinning, corneal epithelium defect and was treated with Acular (View Usage). After Acular was administered, patient had the following side effects: ulcerative keratitis. Acular dosage: 1 Gtt, Qid.

6110152-3 | Corneal Disorder, Glaucoma, Visual Impairment
on Mar 06, 2009 Male patient from UNITED STATES , 79 years of age, weighting 165.0 lb, was diagnosed with retinal oedema and was treated with Acular (View Usage). Patient experienced the following unwanted or unexpected effects: corneal disorder, glaucoma (What is glaucoma?), visual impairment. Acular dosage: Drop On Right Eye Four Times A Day.

5805285-2 | Eye Haemorrhage, Eye Irritation, Eye Pain, Ocular Hyperaemia, Post Procedural Complication
Patient was taking Acular (View Usage). Patient had the following side effects: eye haemorrhage, eye irritation, eye pain, ocular hyperaemia, post procedural complication on Jun 30, 2008 from BRAZIL Additional patient health information: Male patient , 63 years of age, was diagnosed with postoperative care and. Acular dosage: 1 Gtt, Tid. During the same period patient was treated with CILODEX (1 Gtt, Tid) (View Cilodex Review and Cilodex Label ), ATROPINA (1 Gtt, Bid) (View Atropina Review and Atropina Label ), ALPHAGAN (1 Gtt, Tid) (View Alphagan Review and Alphagan Label ).

5793053-X | Eye Haemorrhage, Eye Irritation, Eye Pain, Ocular Hyperaemia
Adverse event was reported on Jun 23, 2008 by a Male patient taking Acular (View Usage) (Dosage: ) was diagnosed with postoperative care and. Location: BRAZIL , 63 years of age, After Acular was administered, patient had the following side effects: eye haemorrhage, eye irritation, eye pain, ocular hyperaemia. During the same period patient was treated with CILODEX (1 Gtt, Tid) (View Cilodex Review and Cilodex Label ), ATROPINA (1 Gtt, Bid) (View Atropina Review and Atropina Label ), ALPHAGAN (1 Gtt, Tid) (View Alphagan Review and Alphagan Label ).

5690877-4 | Blood Glucose Increased, Blood Pressure Increased, Dizziness, Feeling Hot, Hyperhidrosis
on Mar 25, 2008 Male patient from UNITED STATES , weighting 165.0 lb, was diagnosed with preoperative care, diabetes mellitus, hypertension, prostatic disorder and was treated with Acular (View Usage). Patient experienced the following unwanted or unexpected effects: blood glucose increased, blood pressure increased, dizziness (What is dizziness?), feeling hot, hyperhidrosis. Acular dosage: 1 Gtt, Single. During the same period patient was treated with GLUCOPHAGE ER (500 Mg, Tid) (View Glucophage Er Review and Glucophage Er Label ), TOPROL XL (50 Mg, Qhs) (View Toprol-xl Review and Toprol-xl Label ), NIFEDIAC CC (30 Mg, Qam) (View Nifediac Cc Review and Nifediac Cc Label ), AVODART (0.5 Mg, Mon, Wed, Fri) (View Avodart Review and Avodart Label ).

5331251-X | Corneal Perforation, Flat Anterior Chamber Of Eye
on Feb 03, 2006 Female patient from UNITED STATES , 79 years of age, was diagnosed with eye pain and was treated with Acular (View Usage). Patient had the following side effects: corneal perforation, flat anterior chamber of eye. Acular dosage: 1 Gtt, Qid, Ophthalmic. During the same period patient was treated with MURO (View Muro Review and Muro Label ).

5105914-5 | Corneal Disorder
Patient was taking Acular (View Usage). After Acular was administered, patient had the following side effects: corneal disorder on Aug 08, 2006 from UNITED STATES Additional patient health information: Female patient , weighting 130.0 lb, was diagnosed with hypotony of eye, uveitis, dry eye and. Acular dosage: Unk, Tid. During the same period patient was treated with FLAX SEED OIL (View Flax Seed Oil Review and Flax Seed Oil Label ), INFLAMASE /00016202/ (Unk, Tid) (View Inflamase /00016202/ Review and Inflamase /00016202/ Label ), GENTEAL /00445101/ (Unk, Qhs) (View Genteal /00445101/ Review and Genteal /00445101/ Label ).

5100189-5 | Corneal Disorder
Adverse event was reported on Aug 08, 2006 by a Female patient taking Acular (View Usage) (Dosage: Unk, Tid) was diagnosed with hypotony of eye, uveitis, dry eye and. Location: UNITED STATES , weighting 130.0 lb, Patient experienced the following unwanted or unexpected effects: corneal disorder. During the same period patient was treated with FLAX SEED OIL (View Flax Seed Oil Review and Flax Seed Oil Label ), INFLAMASE /00016202/ (Unk, Tid) (View Inflamase /00016202/ Review and Inflamase /00016202/ Label ), GENTEAL /00445101/ (Unk, Qhs) (View Genteal /00445101/ Review and Genteal /00445101/ Label ).

5018817-1 | Corneal Opacity, Corneal Scar, Ulcerative Keratitis, Visual Acuity Reduced
on May 18, 2006 Male patient from UNITED STATES , 33 years of age, was diagnosed with procedural pain and was treated with Acular (View Usage). Patient had the following side effects: corneal opacity, corneal scar, ulcerative keratitis, visual acuity reduced. Acular dosage: 2gtt, Qid, Ophthalmic. During the same period patient was treated with VIGAMOX (2gtt, Tid, Ophthalmic) (View Vigamox Review and Vigamox Label ).

4974842-8 | Ulcerative Keratitis
on Apr 20, 2005 Male patient from UNITED STATES , 70 years of age, weighting 140.0 lb, was treated with Acular (View Usage). After Acular was administered, patient had the following side effects: ulcerative keratitis. Acular dosage: 2 Drop Qid Eye. During the same period patient was treated with PRED FORTE (View Pred Forte Review and Pred Forte Label ), VIGEMOX (View Vigemox Review and Vigemox Label ).

4836847-7 | Dermatitis Exfoliative, Pyrexia, Toxic Skin Eruption
Patient was taking Acular (View Usage). Patient experienced the following unwanted or unexpected effects: dermatitis exfoliative, pyrexia, toxic skin eruption on Nov 02, 2005 from FRANCE Additional patient health information: Female patient , 84 years of age, was diagnosed with macular oedema and. Acular dosage: . During the same period patient was treated with NORSET (View Norset Review and Norset Label ), LANTUS (View Lantus Review and Lantus Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), EURELIX (View Eurelix Review and Eurelix Label ), CARDIOPATCH (View Cardiopatch Review and Cardiopatch Label ), KARDEGIC (View Kardegic Review and Kardegic Label ). Patient was hospitalized.

4809729-4 | Cataract Operation Complication, Eye Pain, Factitious Disorder, Headache, Hypertension, Iatrogenic Injury, Nerve Injury, Refusal Of Treatment By Patient
Adverse event was reported on Oct 13, 2005 by a Female patient taking Acular (View Usage) (Dosage: 1 Drop Qid Eye) was diagnosed with postoperative care and. Location: UNITED STATES , 75 years of age, weighting 150.0 lb, Patient had the following side effects: cataract operation complication, eye pain, factitious disorder, headache (What is headache?), hypertension, iatrogenic injury, nerve injury, refusal of treatment by patient. During the same period patient was treated with FRED FORTE SUSPENSION (View Fred Forte Suspension Review and Fred Forte Suspension Label ), VIGAMOX (View Vigamox Review and Vigamox Label ).

4744465-4 | Amblyopia, Eye Pain, Headache, Hypertension, Nerve Injury, Vision Blurred, Visual Acuity Reduced
on Jul 28, 2005 Female patient from UNITED STATES , 75 years of age, weighting 150.0 lb, was diagnosed with postoperative care and was treated with Acular (View Usage). After Acular was administered, patient had the following side effects: amblyopia, eye pain, headache (What is headache?), hypertension, nerve injury, vision blurred, visual acuity reduced. Acular dosage: 1 Drop Qid Eye. During the same period patient was treated with PRED FORTE (View Pred Forte Review and Pred Forte Label ), VIGAMOX (View Vigamox Review and Vigamox Label ).

4623214-4 | Burning Sensation, Corneal Oedema, Eye Infection, Eye Irritation, Eye Pain, Herpes Simplex, Herpes Zoster
on Mar 14, 2005 Female patient from , 55 years of age, was diagnosed with hypersensitivity and was treated with Acular (View Usage). Patient experienced the following unwanted or unexpected effects: burning sensation, corneal oedema, eye infection (What is eye infection?), eye irritation, eye pain, herpes simplex (What is herpes simplex?), herpes zoster. Acular dosage: 2 Drop Qid Eye.

4612403-0 | Difficulty In Walking, Eye Irritation, Eye Pain, Eye Swelling, Herpes Ophthalmic, Hypersensitivity
Patient was taking Acular (View Usage). Patient had the following side effects: difficulty in walking, eye irritation, eye pain, eye swelling, herpes ophthalmic, hypersensitivity on Mar 08, 2005 from Additional patient health information: Female patient , 55 years of age, was diagnosed with hypersensitivity and. Acular dosage: 2 Drop Qid Eye.

4606830-5 | Difficulty In Walking, Eye Irritation, Eye Oedema, Eye Pain, Hypersensitivity, Lacrimation Increased, Vision Blurred
Adverse event was reported on Mar 01, 2005 by a Female patient taking Acular (View Usage) (Dosage: 2 Drop Qid Eye) was diagnosed with hypersensitivity and. Location: , 55 years of age, After Acular was administered, patient had the following side effects: difficulty in walking, eye irritation, eye oedema, eye pain, hypersensitivity, lacrimation increased, vision blurred.