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Indicate Your Azasite Side Effects
Blister (1)
Blurred Vision, Swelling (1)
Burning Snsation (1)
Dry Eye (1)
Dry Eye,vision Blurred,burning Snsation (1)
Headache (1)
Inflammation (1)
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Common Azasite Side Effects

top 5 Azasite|Blister|Blurred vi|Burning sn|Dry eye|Dry eye,vi|Headache|Inflammati adverse effects>>See All Azasite Side Effects

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Azasite adverse events reported to FDA.

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Summary

FDA Adverse Reports: 36. View All

Azasite FDA safety alerts: No

Reported hospitalizations: 5

Azasite Dosage, Warnings, Usage.

Post Your Unusual Symptoms:

Most Reported
1Rash
2Blurred Vision, Swelling
3Dry Eye,vision Blurred,burning Snsation
4Headache
5Inflammation
6Blister
7Dry Eye
8Vision Blurred
9Burning Snsation
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Often additional risks of using a medication, such as Azasite, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Azasite users, Learn more about unwanted side effects & find ways to reduce them. Browse Azasite Adverse Reports reported to FDA and participate in Azasite discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Azasite. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Azasite Adverse Effect Reports (FDA)

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6667311-0 | Eye Burns, Liquid Product Physical Issue, Overdose
on Apr 01, 2010 Female patient from UNITED STATES , 74 years of age, weighting 160.3 lb, was diagnosed with rosacea (What is rosacea?) and was treated with Azasite (View Usage). Patient experienced the following unwanted or unexpected effects: eye burns, liquid product physical issue, overdose. Azasite dosage: 1 Drop Ea Eye 2 X Day For 2 Days Then 1 Drop Day For 14 Days.

6646094-4 | Accidental Overdose, Blepharitis, Burning Sensation, Eye Irritation, Eye Pruritus, Eyelid Oedema, Hypersensitivity, Ulcerative Keratitis
Patient was taking Azasite (View Usage). Patient had the following side effects: accidental overdose, blepharitis, burning sensation, eye irritation, eye pruritus, eyelid oedema, hypersensitivity, ulcerative keratitis on Mar 03, 2010 from UNITED STATES Additional patient health information: Male patient , 75 years of age, weighting 164.9 lb, was diagnosed with blepharitis, eye infection staphylococcal, eyelid oedema, ocular hyperaemia, ulcerative keratitis and. Azasite dosage: 1 Gtt, Bid, Ophthalmic; 1 Gtt, Qd, Ophthalmic.

6644356-8 | Burning Sensation, Pain
Adverse event was reported on Mar 18, 2010 by a Female patient taking Azasite (View Usage) (Dosage: 1 Qhs Ophthalmic) was diagnosed with eye irritation and. Location: UNITED STATES , 58 years of age, weighting 220.0 lb, After Azasite was administered, patient had the following side effects: burning sensation, pain (What is pain?).

6611175-8 | Eye Irritation, Eye Pain
on Mar 01, 2010 Male patient from UNITED STATES , 83 years of age, weighting 183.0 lb, was diagnosed with dry eye and was treated with Azasite (View Usage). Patient experienced the following unwanted or unexpected effects: eye irritation, eye pain. Azasite dosage: 1 Drop Into Both Eyes Daily.


6609168-X | Eye Irritation, Eye Pain, Foreign Body Sensation In Eyes, Ocular Hyperaemia, Vision Blurred
on Feb 08, 2010 Female patient from UNITED STATES , 56 years of age, weighting 123.9 lb, was treated with Azasite (View Usage). Patient had the following side effects: eye irritation, eye pain, foreign body sensation in eyes, ocular hyperaemia, vision blurred. Azasite dosage: 1 Gtt, Unk, Ophthlamic. During the same period patient was treated with FLAXSEED OIL (LINUM USITATISSIMUM SEED OIL) (View Flaxseed Oil (linum Usitatissimum Seed Oil) Review and Flaxseed Oil (linum Usitatissimum Seed Oil) Label ), FISH OIL (FISH OIL) (View Fish Oil (fish Oil) Review and Fish Oil (fish Oil) Label ), RESTASIS (CICLOSPORIN) (View Restasis (ciclosporin) Review and Restasis (ciclosporin) Label ).

6609166-6 | Blepharitis, Erysipelas, Eye Discharge, Eye Pain, Eye Pruritus, Eye Swelling, Herpes Simplex Ophthalmic, Hypersensitivity, Periorbital Cellulitis
Patient was taking Azasite (View Usage). After Azasite was administered, patient had the following side effects: blepharitis, erysipelas, eye discharge, eye pain, eye pruritus, eye swelling, herpes simplex ophthalmic, hypersensitivity, periorbital cellulitis on Feb 10, 2010 from UNITED STATES Additional patient health information: Female patient , 83 years of age, weighting 127.9 lb, was diagnosed with blepharitis, eye pruritus, eye swelling, hypersensitivity and. Azasite dosage: 2 Gtt, Bid, Ophthalmic 1gtt, Bid, Ophthalmic. During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.

6589837-0 | Blister, Cellulitis, Eye Pain, Eyelid Exfoliation, Eyelids Pruritus, Rash, Swelling
Adverse event was reported on Jan 28, 2010 by a Female patient taking Azasite (View Usage) (Dosage: 2 Gtt, Bid, Ophthalmic, 1 Gtt, Bid, Ophthalmic) was diagnosed with eye pruritus, eye swelling, hypersensitivity and. Location: UNITED STATES , 83 years of age, weighting 127.9 lb, Patient experienced the following unwanted or unexpected effects: blister, cellulitis (What is cellulitis?), eye pain, eyelid exfoliation, eyelids pruritus, rash (What is rash?), swelling. During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), CENTRUM SILVER (VITAMINS NOS, ZINC) (View Centrum Silver (vitamins Nos, Zinc) Review and Centrum Silver (vitamins Nos, Zinc) Label ). Patient was hospitalized.

6589791-1 | Dizziness, Epistaxis, Headache, Nervous System Disorder, Nervousness, Rosacea, Tremor
on Jan 22, 2010 Female patient from UNITED STATES , 83 years of age, weighting 123.9 lb, was diagnosed with dry eye, ocular hyperaemia and was treated with Azasite (View Usage). Patient had the following side effects: dizziness (What is dizziness?), epistaxis, headache (What is headache?), nervous system disorder, nervousness, rosacea (What is rosacea?), tremor. Azasite dosage: 1 Gtt, Qd, Ophthalmic. During the same period patient was treated with BONIVA (View Boniva Review and Boniva Label ), OSCAL (VITAMIN D NOS) (View Oscal (vitamin D Nos) Review and Oscal (vitamin D Nos) Label ), RESTASIS (CICLOSPORIN) (View Restasis (ciclosporin) Review and Restasis (ciclosporin) Label ).

6579523-5 | Diarrhoea, Vomiting
on Feb 09, 2010 Male patient from UNITED STATES , child 4 years of age, weighting 48.00 lb, was diagnosed with hordeolum and was treated with Azasite (View Usage). After Azasite was administered, patient had the following side effects: diarrhoea, vomiting. Azasite dosage: 2 Drops First 2 Days Ophthalmic.

6579504-1 | Injection Site Dermatitis, Injection Site Hypersensitivity
Patient was taking Azasite (View Usage). Patient experienced the following unwanted or unexpected effects: injection site dermatitis, injection site hypersensitivity on Feb 10, 2010 from UNITED STATES Additional patient health information: Male patient , 75 years of age, weighting 250.0 lb, was diagnosed with blepharitis and. Azasite dosage: 1 Drop Ophthalmic.

6575462-4 | Application Site Irritation, Application Site Pain, Dry Eye, Eyelid Oedema, Vision Blurred
Adverse event was reported on Feb 08, 2010 by a Male patient taking Azasite (View Usage) (Dosage: One Drop Twice Daily Ophthalmic (only Used Once)) was diagnosed with eye infection bacterial and. Location: UNITED STATES , 63 years of age, weighting 180.0 lb, Patient had the following side effects: application site irritation, application site pain, dry eye, eyelid oedema, vision blurred.

6523030-2 | Eye Irritation, Eye Pain, Foreign Body Sensation In Eyes, Ocular Hyperaemia
on Dec 04, 2009 Female patient from UNITED STATES , 56 years of age, was treated with Azasite (View Usage). After Azasite was administered, patient had the following side effects: eye irritation, eye pain, foreign body sensation in eyes, ocular hyperaemia. Azasite dosage: 1 Gtt, Ophthalmic.

6489083-5 | Intraocular Pressure Increased
on Nov 24, 2009 Male patient from UNITED STATES , 55 years of age, was treated with Azasite (View Usage). Patient experienced the following unwanted or unexpected effects: intraocular pressure increased. Azasite dosage: Ophthalmic. During the same period patient was treated with AZOPT (View Azopt Review and Azopt Label ), TRAVATAN (View Travatan Review and Travatan Label ).

6415833-X | Pre-eclampsia, Pregnancy, Vision Blurred
Patient was taking Azasite (View Usage). Patient had the following side effects: pre-eclampsia, pregnancy (What is pregnancy?), vision blurred on Oct 08, 2009 from UNITED STATES Additional patient health information: Female patient , 32 years of age, weighting 112.9 lb, was diagnosed with conjunctivitis infective and. Azasite dosage: 1 Gtt, Bid, Ophthalmic. During the same period patient was treated with PRENTAL VITAMINS (ASCORBIC ACID, CALCIUM PANTOTHENATE, CYANOCOBALAMIN, (View Prental Vitamins (ascorbic Acid, Calcium Pantothenate, Cyanocobalamin, Review and Prental Vitamins (ascorbic Acid, Calcium Pantothenate, Cyanocobalamin, Label ). Patient was hospitalized.

6409662-0 | Application Site Irritation, Application Site Pain, Erythema Of Eyelid, Eyelid Oedema, Ocular Hyperaemia, Visual Impairment
Adverse event was reported on Oct 20, 2009 by a Female patient taking Azasite (View Usage) (Dosage: 1 Drop 2 Times A Day After 2 Days One Drop A Day) was diagnosed with blepharitis and. Location: UNITED STATES , 66 years of age, weighting 155.0 lb, After Azasite was administered, patient had the following side effects: application site irritation, application site pain, erythema of eyelid, eyelid oedema, ocular hyperaemia, visual impairment.

6399150-2 | Eye Disorder, Eye Pain, Feeling Hot, Ocular Hyperaemia, Vision Blurred
on Sep 24, 2009 Female patient from UNITED STATES , 56 years of age, weighting 175.0 lb, was treated with Azasite (View Usage). Patient experienced the following unwanted or unexpected effects: eye disorder, eye pain, feeling hot, ocular hyperaemia, vision blurred. Azasite dosage: 1 Gtt, Qd, Ophthalmic. During the same period patient was treated with LOTEMADX (LOTEPREDNOL ETABONATE) (View Lotemadx (loteprednol Etabonate) Review and Lotemadx (loteprednol Etabonate) Label ).

6299552-9 | Accidental Overdose, Deafness, Deafness Unilateral, Ear Discomfort, Eye Discharge, Eye Irritation, Eye Pain, Hypoacusis, Lacrimation Increased
on Jul 16, 2009 Female patient from UNITED STATES , 55 years of age, weighting 140.0 lb, was diagnosed with blepharitis and was treated with Azasite (View Usage). Patient had the following side effects: accidental overdose, deafness, deafness unilateral, ear discomfort, eye discharge, eye irritation, eye pain, hypoacusis, lacrimation increased. Azasite dosage: 1 Gtt, Qd, Ophthalmic. During the same period patient was treated with DOXYCYCLINE (DOXYCYCLINE HYDROCHLORIDE) (View Doxycycline (doxycycline Hydrochloride) Review and Doxycycline (doxycycline Hydrochloride) Label ), ACYCLOVIR (ACICLOVIR SODIUM) (View Acyclovir (aciclovir Sodium) Review and Acyclovir (aciclovir Sodium) Label ).

6284646-4 | Dysphagia, Dyspnoea, Erythema Of Eyelid, Eye Disorder, Madarosis, Multiple Allergies, Ocular Hyperaemia, Skin Tightness, Stevens-johnson Syndrome
Patient was taking Azasite (View Usage). After Azasite was administered, patient had the following side effects: dysphagia, dyspnoea, erythema of eyelid, eye disorder, madarosis, multiple allergies, ocular hyperaemia, skin tightness, stevens-johnson syndrome on Jul 07, 2009 from UNITED STATES Additional patient health information: Female patient , 75 years of age, weighting 134.9 lb, was diagnosed with eye inflammation and. Azasite dosage: 1 Gtt, Bid, Ophthalmic. During the same period patient was treated with CLONIDINE (View Clonidine Review and Clonidine Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), DARVOCET (DEXTROPOXYPHENE HYDROCHLORIDE) (View Darvocet (dextropoxyphene Hydrochloride) Review and Darvocet (dextropoxyphene Hydrochloride) Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ).

6179211-3 | Corneal Erosion, Eye Irritation, Eye Pain, Ocular Hyperaemia, Visual Acuity Reduced
Adverse event was reported on Apr 15, 2009 by a Female patient taking Azasite (View Usage) (Dosage: 1 Gtt, Bid, Ophthalmic) was diagnosed with blepharitis, meibomianitis and. Location: UNITED STATES , 77 years of age, Patient experienced the following unwanted or unexpected effects: corneal erosion, eye irritation, eye pain, ocular hyperaemia, visual acuity reduced. During the same period patient was treated with RESTASIS (CICLOSPORIN) (View Restasis (ciclosporin) Review and Restasis (ciclosporin) Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), MULTIVITAMIN (ZINC) (View Multivitamin (zinc) Review and Multivitamin (zinc) Label ), SYSTANE (MACROGOL, PROPYLENE GLYCOL) (View Systane (macrogol, Propylene Glycol) Review and Systane (macrogol, Propylene Glycol) Label ).

6152741-6 | Corneal Erosion, Eye Irritation, Eye Pain, Ocular Hyperaemia
on Mar 24, 2009 Female patient from UNITED STATES , 77 years of age, was diagnosed with blepharitis, meibomianitis and was treated with Azasite (View Usage). Patient had the following side effects: corneal erosion, eye irritation, eye pain, ocular hyperaemia. Azasite dosage: 1 Gtt, Bid, Ophthalmic. During the same period patient was treated with RESTASIS (CICLOSPORIN) (View Restasis (ciclosporin) Review and Restasis (ciclosporin) Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), MULTIVITAMIN (ZINC) (View Multivitamin (zinc) Review and Multivitamin (zinc) Label ), SYSTANE (MACROGOL, PROPYLENE GLYCOL) (View Systane (macrogol, Propylene Glycol) Review and Systane (macrogol, Propylene Glycol) Label ).

6138975-5 | Blood Pressure Increased, Epistaxis, Nasal Dryness, Stress
on Mar 13, 2009 Female patient from UNITED STATES , 80 years of age, was diagnosed with conjunctivitis and was treated with Azasite (View Usage). After Azasite was administered, patient had the following side effects: blood pressure increased, epistaxis, nasal dryness, stress (What is stress?). Azasite dosage: 1 Gtt, Bid, Ophthalmic. During the same period patient was treated with ZESTRIL (View Zestril Review and Zestril Label ), LUMIGAN (View Lumigan Review and Lumigan Label ), AZOPT (View Azopt Review and Azopt Label ).

6093801-8 | Rash Pruritic
Patient was taking Azasite (View Usage). Patient experienced the following unwanted or unexpected effects: rash pruritic on Feb 22, 2009 from UNITED STATES Additional patient health information: Female patient , 64 years of age, weighting 116.0 lb, was diagnosed with bacterial infection (What is bacterial infection?) and. Azasite dosage: One Eyedrop Daily Ophthalmic.

6046430-6 | Instillation Site Irritation
Adverse event was reported on Jan 21, 2009 by a Female patient taking Azasite (View Usage) (Dosage: 1 Drop Two Times A Day Ophthalmic One Dosage) was diagnosed with dry eye and. Location: UNITED STATES , 54 years of age, weighting 195.0 lb, Patient had the following side effects: instillation site irritation.

5943394-8 | Incorrect Dose Administered, Product Quality Issue
on Nov 05, 2008 Male patient from UNITED STATES , weighting 220.0 lb, was diagnosed with ocular surface disease and was treated with Azasite (View Usage). After Azasite was administered, patient had the following side effects: incorrect dose administered, product quality issue. Azasite dosage: One Drop Ou Bid Ophthalmic.

5941245-9 | Burning Sensation, Pain
on Nov 04, 2008 Male patient from UNITED STATES , 78 years of age, was diagnosed with eye infection (What is eye infection?), infection prophylaxis and was treated with Azasite (View Usage). Patient experienced the following unwanted or unexpected effects: burning sensation, pain (What is pain?). Azasite dosage: 1 Drop Each Eye Bedtime Eyes.

5939572-4 | Visual Acuity Reduced, Visual Field Defect
Patient was taking Azasite (View Usage). Patient had the following side effects: visual acuity reduced, visual field defect on Oct 15, 2008 from UNITED STATES Additional patient health information: Female patient , 79 years of age, was diagnosed with blepharitis and. Azasite dosage: 1 Gtt, Single, Opthalmic. During the same period patient was treated with THYROID TAB (View Thyroid Tab Review and Thyroid Tab Label ), AMBIEN (View Ambien Review and Ambien Label ), ACTONEL (View Actonel Review and Actonel Label ), VITAMIN C (SODIUM ASCORBATE) (View Vitamin C (sodium Ascorbate) Review and Vitamin C (sodium Ascorbate) Label ), VITAMIN B12 (HYDROXOCOBALAMIN ACETATE) (View Vitamin B12 (hydroxocobalamin Acetate) Review and Vitamin B12 (hydroxocobalamin Acetate) Label ).

5908671-5 | Endophthalmitis, Staphylococcal Infection
Adverse event was reported on Sep 11, 2008 by a Female patient taking Azasite (View Usage) (Dosage: 1 Gtt, Qd, Opthalmic) was diagnosed with prophylaxis and. Location: UNITED STATES , 79 years of age, After Azasite was administered, patient had the following side effects: endophthalmitis, staphylococcal infection (What is staphylococcal infection?). During the same period patient was treated with NEXIUM (ESOMEPRAZOLE SODIUM) (View Nexium (esomeprazole Sodium) Review and Nexium (esomeprazole Sodium) Label ), VITEYES (View Viteyes Review and Viteyes Label ).

5892231-9 | Blood Pressure Increased, Dizziness, Headache, Loss Of Consciousness, Toothache, Vision Blurred, Vomiting
on Sep 03, 2008 Female patient from UNITED STATES , 69 years of age, weighting 132.0 lb, was diagnosed with blepharitis and was treated with Azasite (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, dizziness (What is dizziness?), headache (What is headache?), loss of consciousness, toothache, vision blurred, vomiting. Azasite dosage: 1 Gtt Qd Opthalmic. During the same period patient was treated with VITAMINS (View Vitamins Review and Vitamins Label ). Patient was hospitalized.

5874642-0 | Anger, Economic Problem
on Sep 08, 2008 Female patient from UNITED STATES , 68 years of age, weighting 180.0 lb, was treated with Azasite (View Usage). Patient had the following side effects: anger, economic problem. Azasite dosage: .

5871389-1 | Application Site Irritation, Eye Inflammation, Eye Swelling
Patient was taking Azasite (View Usage). After Azasite was administered, patient had the following side effects: application site irritation, eye inflammation, eye swelling on Sep 04, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 182.0 lb, was diagnosed with eye infection (What is eye infection?) and. Azasite dosage: One Drop Bedtime Eye.

5857517-2 | Conjunctival Hyperaemia, Ectropion, Erythema, Eye Swelling, Hypersensitivity, Scleral Disorder, Thermal Burn, Vision Blurred
Adverse event was reported on Aug 08, 2008 by a Female patient taking Azasite (View Usage) (Dosage: Unk, Unk, Opthalmic) was diagnosed with eye infection (What is eye infection?) and. Location: UNITED STATES , 50 years of age, weighting 274.9 lb, Patient experienced the following unwanted or unexpected effects: conjunctival hyperaemia, ectropion, erythema, eye swelling, hypersensitivity, scleral disorder, thermal burn, vision blurred. During the same period patient was treated with PROTONIX (View Protonix Review and Protonix Label ), CYCLOBENZAPRINE HYDROCHLORIDE (View Cyclobenzaprine Hydrochloride Review and Cyclobenzaprine Hydrochloride Label ), SUDAFED 12 HOUR (View Sudafed 12 Hour Review and Sudafed 12 Hour Label ), GENTEAL (UROGASTRONE) (View Genteal (urogastrone) Review and Genteal (urogastrone) Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ).

5846002-X | Ectropion, Erythema, Eye Swelling, Hypersensitivity, Vision Blurred
on Jul 28, 2008 Female patient from UNITED STATES , 50 years of age, weighting 274.9 lb, was diagnosed with eye infection (What is eye infection?) and was treated with Azasite (View Usage). Patient had the following side effects: ectropion, erythema, eye swelling, hypersensitivity, vision blurred. Azasite dosage: Opthalmic. During the same period patient was treated with PROTONIX (PANTAPRAZOLE SODIUM) (View Protonix (pantaprazole Sodium) Review and Protonix (pantaprazole Sodium) Label ), CYCLOBENZAPRINE HYDROCHLORIDE (View Cyclobenzaprine Hydrochloride Review and Cyclobenzaprine Hydrochloride Label ), SUDAFED 12 HOUR (View Sudafed 12 Hour Review and Sudafed 12 Hour Label ), GENTEAL (UROGASTRONE) (View Genteal (urogastrone) Review and Genteal (urogastrone) Label ).

5795355-X | Blister, Eye Swelling, Herpes Zoster, Pruritus, Swelling Face, Visual Acuity Reduced
on Jun 10, 2008 Female patient from UNITED STATES , 84 years of age, weighting 110.0 lb, was diagnosed with dry eye, eye infection (What is eye infection?) and was treated with Azasite (View Usage). After Azasite was administered, patient had the following side effects: blister, eye swelling, herpes zoster, pruritus, swelling face, visual acuity reduced. Azasite dosage: 1 Gtt, Qd, Opthalmic. During the same period patient was treated with PRAVASTATIN SODIUM (View Pravastatin Sodium Review and Pravastatin Sodium Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), MULTIVITAMIN (View Multivitamin Review and Multivitamin Label ), FLAXSEED OIL (LINUM USITATISSIMUM SEED OIL) (View Flaxseed Oil (linum Usitatissimum Seed Oil) Review and Flaxseed Oil (linum Usitatissimum Seed Oil) Label ), CALCIUM (CALCIUM) (View Calcium (calcium) Review and Calcium (calcium) Label ), RESTASIS (CICLOSPORIN) (View Restasis (ciclosporin) Review and Restasis (ciclosporin) Label ), REFRESH PLUS (CARMELLOSE SODIUM, MAGNESIUM CHLORIDE ANHYDROUS, POTASSI (View Refresh Plus (carmellose Sodium, Magnesium Chloride Anhydrous, Potassi Review and Refresh Plus (carmellose Sodium, Magnesium Chloride Anhydrous, Potassi Label ).

5647941-5 | Corneal Disorder, Corneal Perforation, Corneal Transplant, Impaired Healing, Ulcerative Keratitis
Patient was taking Azasite (View Usage). Patient experienced the following unwanted or unexpected effects: corneal disorder, corneal perforation, corneal transplant, impaired healing, ulcerative keratitis on Feb 13, 2008 from UNITED STATES Additional patient health information: Male patient , 57 years of age, was diagnosed with eye infection (What is eye infection?), eye inflammation and. Azasite dosage: Opthalmic. During the same period patient was treated with DEXAMETHASONE TAB (View Dexamethasone Tab Review and Dexamethasone Tab Label ), DOXYCYCLINE (DOXYCYCLINE HYDROCHLORIDE) (View Doxycycline (doxycycline Hydrochloride) Review and Doxycycline (doxycycline Hydrochloride) Label ), CYTOXAN (View Cytoxan Review and Cytoxan Label ), VIGAMOX (View Vigamox Review and Vigamox Label ).

5627146-4 | Eye Discharge, Instillation Site Irritation, Skin Irritation
Adverse event was reported on Feb 12, 2008 by a Female patient taking Azasite (View Usage) (Dosage: 2 Gtts In Effected Eye Bid X 2 Days Ophthalmic 1 Gtt In Effected Eye Daily X 5 Days Ophthalmic) was diagnosed with conjunctivitis bacterial and. Location: UNITED STATES , weighting 115.0 lb, Patient had the following side effects: eye discharge, instillation site irritation, skin irritation.

5517857-3 | Cerebrovascular Accident, Fall
on Oct 25, 2007 Female patient from UNITED STATES , 78 years of age, was diagnosed with eye operation and was treated with Azasite (View Usage). After Azasite was administered, patient had the following side effects: cerebrovascular accident, fall (What is fall?). Azasite dosage: 1gtt, Tid, Opthalmic. During the same period patient was treated with XIBROM (BROMFENAC SODIUM) (View Xibrom (bromfenac Sodium) Review and Xibrom (bromfenac Sodium) Label ), ECONOPRED (PREDNISOLONE ACETATE) (View Econopred (prednisolone Acetate) Review and Econopred (prednisolone Acetate) Label ). Patient was hospitalized.


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Azasite Questions, Answers, Feedback and Comments

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Azasite risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Azasite quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Azasite use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Azasite Reactions
Accidental Overdose
Application Site Irritation
Application Site Pain
Blepharitis
Blister
Blood Pressure Increased
Burning Sensation
Corneal Erosion
DizzinessWhat is Dizziness?
Ectropion
Epistaxis
Erythema
Erythema Of Eyelid
Eye Discharge
Eye Disorder
Eye Irritation
Eye Pain
Eye Pruritus
Eye Swelling
Eyelid Oedema
Foreign Body Sensation In Eyes
HeadacheWhat is Headache?
Hypersensitivity
Instillation Site Irritation
Ocular Hyperaemia
PainWhat is Pain?
Ulcerative Keratitis
Vision Blurred
Visual Acuity Reduced
Vomiting
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