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Alcaine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 8. View All

Alcaine FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 2

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Often additional risks of using a medication, such as Alcaine, 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 Alcaine users, Learn more about unwanted side effects & find ways to reduce them. Browse Alcaine Adverse Reports reported to FDA and participate in Alcaine discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Alcaine. 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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Alcaine Adverse Effect Reports (FDA)

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6538028-8 | Asthenia, Blood Pressure Decreased, Haemodynamic Instability, Hyperhidrosis, Loss Of Consciousness, Tremor
on Dec 29, 2009 Male patient from UKRAINE , 38 years of age, was diagnosed with foreign body in eye and was treated with Alcaine (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, blood pressure decreased, haemodynamic instability, hyperhidrosis, loss of consciousness, tremor. Alcaine dosage: 1 Gtt Once Ophthalmic.

6472824-0 | Asthenia, Blood Pressure Decreased, Hyperhidrosis, Loss Of Consciousness, Tremor
Patient was taking Alcaine (View Usage). Patient had the following side effects: asthenia, blood pressure decreased, hyperhidrosis, loss of consciousness, tremor on Nov 23, 2009 from UKRAINE Additional patient health information: Male patient , 38 years of age, was diagnosed with foreign body in eye and. Alcaine dosage: 1 Gtt Once Ophthalmic.

5155550-X | Application Site Reaction, Hypersensitivity, Visual Disturbance
Adverse event was reported on Oct 27, 2006 by a Female patient taking Alcaine (View Usage) (Dosage: ) . Location: UNITED STATES , 48 years of age, After Alcaine was administered, patient had the following side effects: application site reaction, hypersensitivity, visual disturbance.

5100523-6 | Application Site Pain, Heart Rate Decreased, Postictal State, Tonic Clonic Movements, Unresponsive To Stimuli
on Sep 07, 2006 Male patient from UNITED STATES , 41 years of age, weighting 230.0 lb, was diagnosed with eye injury and was treated with Alcaine (View Usage). Patient experienced the following unwanted or unexpected effects: application site pain, heart rate decreased, postictal state, tonic clonic movements, unresponsive to stimuli. Alcaine dosage: 2 Drops Once Ophthalmic. During the same period patient was treated with FLUORETS CHAUVIN (1 Unit Once Ophthalmic) (View Fluorets Chauvin Review and Fluorets Chauvin Label ).


5083743-9 | Emphysema, Myocardial Infarction, Pain, Purulence, Pyelonephritis
on Jul 28, 2006 Female patient from BRAZIL , 40 years of age, was diagnosed with intraocular pressure test, fundoscopy and was treated with Alcaine (View Usage). Patient had the following side effects: emphysema, myocardial infarction, pain (What is pain?), purulence, pyelonephritis. Alcaine dosage: Opht. During the same period patient was treated with MYDRIACYL (Opht) (View Mydriacyl Review and Mydriacyl Label ), FLUORESCEIN SODIUM (View Fluorescein Sodium Review and Fluorescein Sodium Label ).

5067641-2 | Cardiac Arrest, Malaise, Myocardial Infarction
Patient was taking Alcaine (View Usage). After Alcaine was administered, patient had the following side effects: cardiac arrest (What is cardiac arrest?), malaise, myocardial infarction on Jul 13, 2006 from BRAZIL Additional patient health information: Female patient , 41 years of age, was diagnosed with intraocular pressure test, fundoscopy and. Alcaine dosage: Opht {1 Month. During the same period patient was treated with MYDRIACYL (Opht) (View Mydriacyl Review and Mydriacyl Label ).

4996137-9 | Conjunctival Hyperaemia, Corneal Epithelium Defect, Corneal Infiltrates, Corneal Neovascularisation, Factitious Disorder, Keratopathy, Major Depression
Adverse event was reported on Apr 21, 2006 by a Female patient taking Alcaine (View Usage) (Dosage: ) . Location: UNITED STATES , 21 years of age, Patient experienced the following unwanted or unexpected effects: conjunctival hyperaemia, corneal epithelium defect, corneal infiltrates, corneal neovascularisation, factitious disorder, keratopathy, major depression. Patient was hospitalized and became disabled.

4996136-7 | Blepharitis, Conjunctival Hyperaemia, Corneal Epithelium Defect, Corneal Infiltrates, Dermatitis Contact, Eye Pain, Factitious Disorder, Hypopyon
on Apr 21, 2006 Female patient from UNITED STATES , 19 years of age, was treated with Alcaine (View Usage). Patient had the following side effects: blepharitis, conjunctival hyperaemia, corneal epithelium defect, corneal infiltrates, dermatitis contact, eye pain, factitious disorder, hypopyon. Alcaine dosage: . Patient was hospitalized and became disabled.


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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 Alcaine 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 Alcaine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Alcaine 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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Alcaine Reactions
Application Site Pain
Application Site Reaction
Asthenia
Blepharitis
Blood Pressure Decreased
Cardiac ArrestWhat is Cardiac arrest?
Conjunctival Hyperaemia
Corneal Epithelium Defect
Corneal Infiltrates
Corneal Neovascularisation
Dermatitis Contact
Emphysema
Eye Pain
Factitious Disorder
Haemodynamic Instability
Heart Rate Decreased
Hyperhidrosis
Hypersensitivity
Hypopyon
Keratopathy
Loss Of Consciousness
Major Depression
Malaise
Myocardial Infarction
PainWhat is Pain?
Postictal State
Purulence
Pyelonephritis
Tonic Clonic Movements
Tremor
Alcaine Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Alcaine adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!