IOPIDINE Side Effects

6963865-5 | Blood Pressure Increased, Heart Rate Decreased, Pallor, Pulmonary Oedema, Somnolence
on Aug 18, 2010 Female patient from UNITED KINGDOM , child 6 years of age, was diagnosed with vasoconstriction and was treated with Iopidine (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, heart rate decreased, pallor, pulmonary oedema, somnolence. Iopidine dosage: 1 Gtt; Ophthalmic. During the same period patient was treated with PROPFOL (View Propfol Review and Propfol Label ), REMIFENTANIL (View Remifentanil Review and Remifentanil Label ), GLYCOPYRROLATE (View Glycopyrrolate Review and Glycopyrrolate Label ). Patient was hospitalized.

6686871-7 | Hypertension, Oxygen Saturation Decreased, Pulmonary Oedema, Somnolence
Patient was taking Iopidine (View Usage). Patient had the following side effects: hypertension, oxygen saturation decreased, pulmonary oedema, somnolence on Apr 06, 2010 from UNITED KINGDOM Additional patient health information: Female patient , child 5 years of age, was diagnosed with vasoconstriction and. Iopidine dosage: 1gtt. During the same period patient was treated with GLYCOPYRROLATE (GLYCOPYRRONIUM) (View Glycopyrrolate (glycopyrronium) Review and Glycopyrrolate (glycopyrronium) Label ). Patient was hospitalized.

6655303-7 | Hypertension, Oxygen Saturation Decreased, Pulmonary Oedema, Somnolence
Adverse event was reported on Mar 12, 2010 by a Female patient taking Iopidine (View Usage) (Dosage: Gtt Ophthalmic) was diagnosed with vasoconstriction and. Location: UNITED KINGDOM , child 5 years of age, After Iopidine was administered, patient had the following side effects: hypertension, oxygen saturation decreased, pulmonary oedema, somnolence. During the same period patient was treated with PROPOFOL (View Propofol Review and Propofol Label ), REMIFENTANIL (REMIFENTANIL) (View Remifentanil (remifentanil) Review and Remifentanil (remifentanil) Label ), GLYCOPYRROLATE (GLYCOPYRRONIUM) (View Glycopyrrolate (glycopyrronium) Review and Glycopyrrolate (glycopyrronium) Label ). Patient was hospitalized.

6537087-6 | Miosis, Retinal Haemorrhage, Retinopathy, Visual Acuity Reduced
on Dec 23, 2009 Female patient from UNITED KINGDOM , 65 years of age, was diagnosed with angle closure glaucoma and was treated with Iopidine (View Usage). Patient experienced the following unwanted or unexpected effects: miosis, retinal haemorrhage, retinopathy, visual acuity reduced. Iopidine dosage: Ophthalmic. During the same period patient was treated with MAXIDEX FORTE DROPS (Ophthalmic) (View Maxidex Forte Drops Review and Maxidex Forte Drops Label ), PILOCARPINE HCL (Ophthalmic) (View Pilocarpine Hcl Review and Pilocarpine Hcl Label ), ACETAZOLAMIDE (View Acetazolamide Review and Acetazolamide Label ). Patient was hospitalized.


6497541-2 | Miosis, Retinal Haemorrhage, Retinopathy
on Dec 10, 2009 Female patient from UNITED KINGDOM , 65 years of age, was diagnosed with angle closure glaucoma and was treated with Iopidine (View Usage). Patient had the following side effects: miosis, retinal haemorrhage, retinopathy. Iopidine dosage: Ophthalmic. During the same period patient was treated with MAXIDEX FORTE DROPS (Ophthalmic) (View Maxidex Forte Drops Review and Maxidex Forte Drops Label ), PILOCARPINE HCL (Ophthalmic) (View Pilocarpine Hcl Review and Pilocarpine Hcl Label ), ACETAZOLAMIDE (View Acetazolamide Review and Acetazolamide Label ). Patient was hospitalized.

6220175-1 | Circulatory Collapse
Patient was taking Iopidine (View Usage). After Iopidine was administered, patient had the following side effects: circulatory collapse on May 26, 2009 from FRANCE Additional patient health information: Female patient , 77 years of age, . Iopidine dosage: Ophthalmic. During the same period patient was treated with ISOPTIN (View Isoptin Review and Isoptin Label ), ZOCOR (View Zocor Review and Zocor Label ). Patient was hospitalized.

6008915-8 | Pupillary Reflex Impaired, Treatment Noncompliance, Vision Blurred
Adverse event was reported on Dec 01, 2008 by a Male patient taking Iopidine (View Usage) (Dosage: 1 Gtt Ou X 1 Ophthalmic, (1 Gtt Ou X 1 Ophthalmic)) was diagnosed with intraocular pressure increased and. Location: UNITED STATES , 49 years of age, Patient experienced the following unwanted or unexpected effects: pupillary reflex impaired, treatment noncompliance, vision blurred. During the same period patient was treated with TRAVATAN (1 Gtt Ou Q Hs, Ophthalmic) (View Travatan Review and Travatan Label ), TIMOLOL MALEATE (1 Gtt Ou Qd, Ophthalmic) (View Timolol Maleate Review and Timolol Maleate Label ), BRIMONIDINE TARTRATE (View Brimonidine Tartrate Review and Brimonidine Tartrate Label ).

5874065-4 | Hypertension, Oxygen Saturation Decreased, Pulmonary Oedema, Somnolence
on Aug 13, 2008 Female patient from UNITED KINGDOM , child 5 years of age, was diagnosed with vasoconstriction and was treated with Iopidine (View Usage). Patient had the following side effects: hypertension, oxygen saturation decreased, pulmonary oedema, somnolence. Iopidine dosage: 1 Gtt. During the same period patient was treated with PROPOFOL (View Propofol Review and Propofol Label ), REMIFENTANIL (REMIFENTANIL) (View Remifentanil (remifentanil) Review and Remifentanil (remifentanil) Label ), GLYCOPYRROLATE (GLYCOPYRROLATE) (View Glycopyrrolate (glycopyrrolate) Review and Glycopyrrolate (glycopyrrolate) Label ). Patient was hospitalized.

5874060-5 | Bradycardia, Hypertension, Lethargy
on Aug 13, 2008 Male patient from UNITED KINGDOM , child 5 years of age, was diagnosed with vasoconstriction and was treated with Iopidine (View Usage). After Iopidine was administered, patient had the following side effects: bradycardia, hypertension, lethargy. Iopidine dosage: 1 Gtt Ou. During the same period patient was treated with PROPOFOL (View Propofol Review and Propofol Label ), REMIFENTANIL (REMIFENTANIL) (View Remifentanil (remifentanil) Review and Remifentanil (remifentanil) Label ), GLYCOPYRROLATE (GLYCOPYRRONIUM) (View Glycopyrrolate (glycopyrronium) Review and Glycopyrrolate (glycopyrronium) Label ).

5758099-6 | Abasia, Depressed Level Of Consciousness, Lethargy, Oxygen Saturation Decreased, Pallor, Respiratory Rate Increased, Somnolence
Patient was taking Iopidine (View Usage). Patient experienced the following unwanted or unexpected effects: abasia, depressed level of consciousness, lethargy, oxygen saturation decreased, pallor, respiratory rate increased, somnolence on May 16, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 30.86 lb, . Iopidine dosage: Oral. Patient was hospitalized.

5713687-8 | Loss Of Consciousness, Shock
Adverse event was reported on Apr 02, 2008 by a Female patient taking Iopidine (View Usage) (Dosage: 1 Gtt 30 Min Prior To Surgery Opthalmic) was diagnosed with eye laser surgery and. Location: JAPAN , 86 years of age, Patient had the following side effects: loss of consciousness, shock. During the same period patient was treated with MYDRIN P(MYDRIN P) (View Mydrin P(mydrin P) Review and Mydrin P(mydrin P) Label ).

5688219-3 | Blood Pressure Decreased, Loss Of Consciousness
on Mar 14, 2008 Female patient from JAPAN , 80 years of age, was diagnosed with eye laser surgery and was treated with Iopidine (View Usage). After Iopidine was administered, patient had the following side effects: blood pressure decreased, loss of consciousness. Iopidine dosage: . During the same period patient was treated with MYDRIN (ISOCOM) (View Mydrin (isocom) Review and Mydrin (isocom) Label ).

5168486-5 | Myocardial Infarction
on Nov 16, 2006 Male patient from JAPAN , 73 years of age, was diagnosed with inflammation and was treated with Iopidine (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction. Iopidine dosage: Opht. During the same period patient was treated with DORZOLAMIDE HYDROCHLORIDE (View Dorzolamide Hydrochloride Review and Dorzolamide Hydrochloride Label ), DEXAMETHASONE 0.1% SUSPENSION (View Dexamethasone 0.1% Suspension Review and Dexamethasone 0.1% Suspension Label ). Patient was hospitalized.

4808905-4 | Accidental Overdose, Anaemia, Asthenia, Blood Pressure Increased, Blood Urea Increased, Bradycardia, Depressed Level Of Consciousness, Dysarthria, Headache
Patient was taking Iopidine (View Usage). Patient had the following side effects: accidental overdose, anaemia, asthenia, blood pressure increased, blood urea increased, bradycardia, depressed level of consciousness, dysarthria, headache (What is headache?) on Oct 06, 2005 from TURKEY Additional patient health information: Female patient , 56 years of age, was diagnosed with intraocular pressure increased, prophylaxis and. Iopidine dosage: 5 Ml Over 12 Hours, Opht. During the same period patient was treated with LOSARTAN (View Losartan Review and Losartan Label ). Patient was hospitalized.