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Did You Have a Olopatadine Side Effect? How Effective is Olopatadine for You? |
Olopatadine Forum |
Olopatadine Adverse Effect Reports (FDA)
Showing 1-25 of 27 Next Page >
Renal Impairment (8453938-2)
on Jun 06, 2012 Male patient from JAPAN , 42 years of age, was treated with Olopatadine Hcl(View Usage). Patient experienced the following unwanted or unexpected effects: renal impairment. Olopatadine Hcl dosage: Unk.
Patient was taking other medications:
Blood Potassium Increased, Renal Disorder, Haemoglobin Decreased, Acute Respiratory Failure, Blood Creatinine Increased, Haematocrit Decreased, Blood Alkaline Phosphatase Increased, Blood Urea Increased (8389910-0)
Patient was taking Olopatadine Hcl (View Usage). Patient had the following side effects: blood potassium increased, renal disorder, haemoglobin decreased, acute respiratory failure, blood creatinine increased, haematocrit decreased, blood alkaline phosphatase increased, blood urea increased on May 08, 2012 from JAPAN Additional patient health information: Male patient , 78 years of age, . Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
Toxic Skin Eruption (8385896-3)
Adverse event was reported on May 17, 2012 by a Female patient taking Olopatadine Hcl (View Usage) (Dosage: N/A) . Location: JAPAN , 69 years of age, weighting 88.18 lb, After Olopatadine was administered, patient had the following side effects: toxic skin eruption.
Patient was taking other medications:
Aggression, Suicide Attempt (8334843-9)
on Apr 23, 2012 Female patient from JAPAN , 39 years of age, was diagnosed with
Patient was taking other medications:
Juvenile Arthritis, Hepatic Function Abnormal (8323395-5)
on Apr 27, 2012 Female patient from JAPAN , weighting 103.6 lb, was diagnosed with
Patient was taking other medications:
Haematocrit Increased, Leukocytosis, Chronic Myeloid Leukaemia (8125354-4)
Patient was taking Olopatadine Hcl (View Usage). After Olopatadine was administered, patient had the following side effects: haematocrit increased, leukocytosis, chronic myeloid leukaemia on Jan 30, 2012 from JAPAN Additional patient health information: Male patient , weighting 211.6 lb, was diagnosed with
Patient was taking other medications:
Loss Of Consciousness, Nausea (8105502-2)
Adverse event was reported on Jan 30, 2012 by a Female patient taking Olopatadine Hcl (View Usage) (Dosage: 10 Mg, 1x/day) . Location: JAPAN , 69 years of age, Patient experienced the following unwanted or unexpected effects: loss of consciousness, nausea (nausea Questions).
Patient was taking other medications:
Hepatic Neoplasm Malignant, Pyrexia, Neutrophil Count Increased, Hepatic Function Abnormal, Insomnia, Hypertension, Constipation (8065380-7)
on Jan 20, 2012 Male patient from JAPAN , 54 years of age, weighting 138.9 lb, was treated with Olopatadine Hcl (View Usage). Patient had the following side effects: hepatic neoplasm malignant, pyrexia, neutrophil count increased, hepatic function abnormal, insomnia, hypertension, constipation (constipation Questions). Olopatadine Hcl dosage: Daily Dose 10 Mg.
Patient was taking other medications:
Blood Glucose Increased (8029858-4)
on Dec 27, 2011 Male patient from JAPAN , 73 years of age, weighting 154.3 lb, was treated with Olopatadine Hcl(View Usage). After Olopatadine was administered, patient had the following side effects: blood glucose increased. Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
Blood Albumin Decreased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Epstein-barr Virus Antibody Positive, Faeces Pale, Allergic Hepatitis, Prothrombin Time Prolonged, Malaise, Prothrombin Time Ratio Decreased (8018605-8)
Patient was taking Olopatadine Hcl (View Usage). Patient experienced the following unwanted or unexpected effects: blood albumin decreased, aspartate aminotransferase increased, blood lactate dehydrogenase increased, epstein-barr virus antibody positive, faeces pale, allergic hepatitis, prothrombin time prolonged, malaise, prothrombin time ratio decreased on Dec 20, 2011 from JAPAN Additional patient health information: Female patient , 81 years of age, was diagnosed with
Patient was taking other medications:
Laceration (8007206-3)
Adverse event was reported on Dec 13, 2011 by a Female patient taking Olopatadine Hcl (View Usage) (Dosage: 5 Mg, 2x/day) was diagnosed with
Patient was taking other medications:
Pain, Myocardial Infarction, Cerebrovascular Accident, Pulmonary Embolism, Anxiety, Gallbladder Disorder, Deep Vein Thrombosis, Cholecystitis Acute, Cholecystitis Chronic (7912392-7)
on Nov 04, 2011 Female patient from UNITED STATES , 25 years of age, weighting 135.0 lb, was treated with Olopatadine Hydrochloride (View Usage). After Olopatadine was administered, patient had the following side effects: pain (pain Questions), myocardial infarction, cerebrovascular accident, pulmonary embolism (pulmonary embolism Questions), anxiety (anxiety Questions), gallbladder disorder, deep vein thrombosis (deep vein thrombosis Questions), cholecystitis acute, cholecystitis chronic. Olopatadine Hydrochloride dosage: Unk Unk, Prn.
Patient was taking other medications:
Dyspnoea, Burning Sensation (7850789-4)
on Oct 19, 2011 Male patient from UNITED STATES , weighting 195.2 lb, was diagnosed with
Patient was taking other medications:
Pulmonary Artery Thrombosis, Venous Thrombosis (7833499-9)
Patient was taking Olopatadine Hcl (View Usage). Patient had the following side effects: pulmonary artery thrombosis, venous thrombosis on Oct 12, 2011 from JAPAN Additional patient health information: Female patient , 29 years of age, weighting 132.3 lb, was diagnosed with
Patient was taking other medications:
Jaw Disorder, Paralysis, Viith Nerve Paralysis, Apraxia, Tenderness, Cranial Nerve Palsies Multiple, Temporomandibular Joint Syndrome, Dysphagia, Trismus (7817466-7)
Adverse event was reported on Oct 03, 2011 by a Male patient taking Olopatadine Hcl (View Usage) (Dosage: N/A) . Location: JAPAN , 75 years of age, After Olopatadine was administered, patient had the following side effects: jaw disorder, paralysis (paralysis Questions), viith nerve paralysis, apraxia, tenderness, cranial nerve palsies multiple, temporomandibular joint syndrome, dysphagia, trismus.
Patient was taking other medications:
Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Hepatic Function Abnormal (7814212-8)
on Oct 04, 2011 Male patient from JAPAN , 71 years of age, weighting 160.9 lb, was treated with Olopatadine Hcl (View Usage). Patient experienced the following unwanted or unexpected effects: aspartate aminotransferase increased, alanine aminotransferase increased, hepatic function abnormal. Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
White Blood Cell Count Increased, Haematocrit Increased (7802479-1)
on Sep 29, 2011 Male patient from JAPAN , weighting 211.6 lb, was diagnosed with
Patient was taking other medications:
Thyroid Cancer (7777138-4)
Patient was taking Olopatadine Hcl (View Usage). After Olopatadine was administered, patient had the following side effects: thyroid cancer (thyroid cancer Questions) on Sep 13, 2011 from JAPAN Additional patient health information: Female patient , 37 years of age, weighting 179.0 lb, . Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
Dermatitis Bullous (7704364-2)
Adverse event was reported on Aug 15, 2011 by a Female patient taking Olopatadine Hcl (View Usage) (Dosage: N/A) was diagnosed with
Patient was taking other medications:
Thrombotic Cerebral Infarction, Decreased Appetite (7585927-4)
on Jun 20, 2011 Female patient from JAPAN , 77 years of age, weighting 108.0 lb, was diagnosed with
Patient was taking other medications:
Aspartate Aminotransferase Increased, Hypersensitivity, Alanine Aminotransferase Increased, Eczema Asteatotic, Lymphocyte Count Decreased, Blood Amylase Increased, Rash, Blood Creatinine Increased (7561801-4)
on Jun 14, 2011 Male patient from JAPAN , weighting 121.3 lb, was treated with Olopatadine(View Usage). After Olopatadine was administered, patient had the following side effects: aspartate aminotransferase increased, hypersensitivity, alanine aminotransferase increased, eczema asteatotic, lymphocyte count decreased, blood amylase increased, rash (rash Questions), blood creatinine increased. Olopatadine dosage: N/A.
Patient was taking other medications:
Hepatitis Acute (7554037-4)
Patient was taking Olopatadine Hcl (View Usage). Patient experienced the following unwanted or unexpected effects: hepatitis acute on Jun 14, 2011 from JAPAN Additional patient health information: Male patient , 22 years of age, . Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
Product Formulation Issue, Bone Pain, Asthenia, Viral Infection (7357691-5)
Adverse event was reported on Jul 14, 2010 by a Male patient taking Olopatadine (View Usage) (Dosage: N/A) . Location: UNITED STATES , 54 years of age, Patient had the following side effects: product formulation issue, bone pain, asthenia, viral infection (viral infection Questions).
Patient was taking other medications:
White Blood Cell Count Increased, Pain Of Skin, Pyrexia, Mobility Decreased, Arthralgia, Hyperuricaemia, C-reactive Protein Increased, Erythrodermic Psoriasis (7315620-4)
on Feb 23, 2011 Male patient from JAPAN , 51 years of age, weighting 187.4 lb, was diagnosed with
Patient was taking other medications:
Breast Cancer (6085275-8)
on Jan 05, 2008 Male patient from UNITED STATES , 88 years of age, weighting 160.0 lb, was diagnosed with
Patient was taking other medications:
on Jun 06, 2012 Male patient from JAPAN , 42 years of age, was treated with Olopatadine Hcl(View Usage). Patient experienced the following unwanted or unexpected effects: renal impairment. Olopatadine Hcl dosage: Unk.
Patient was taking other medications:
- LIPITOR (View Lipitor Review and Lipitor Label )
- DIOVAN (Unk) (View Diovan Review and Diovan Label )
- ALLEGRA (Unk) (View Allegra Review and Allegra Label )
Blood Potassium Increased, Renal Disorder, Haemoglobin Decreased, Acute Respiratory Failure, Blood Creatinine Increased, Haematocrit Decreased, Blood Alkaline Phosphatase Increased, Blood Urea Increased (8389910-0)
Patient was taking Olopatadine Hcl (View Usage). Patient had the following side effects: blood potassium increased, renal disorder, haemoglobin decreased, acute respiratory failure, blood creatinine increased, haematocrit decreased, blood alkaline phosphatase increased, blood urea increased on May 08, 2012 from JAPAN Additional patient health information: Male patient , 78 years of age, . Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
- LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label )
- LOXONIN (View Loxonin Review and Loxonin Label )
- GLUFAST (View Glufast Review and Glufast Label )
- ANTEBATE (View Antebate Review and Antebate Label )
- PREDNISOLONE (View Prednisolone Review and Prednisolone Label )
Toxic Skin Eruption (8385896-3)
Adverse event was reported on May 17, 2012 by a Female patient taking Olopatadine Hcl (View Usage) (Dosage: N/A) . Location: JAPAN , 69 years of age, weighting 88.18 lb, After Olopatadine was administered, patient had the following side effects: toxic skin eruption.
Patient was taking other medications:
- GALANTAMINE HYDROBROMIDE (View Galantamine Hydrobromide Review and Galantamine Hydrobromide Label )
- ASPIRIN DIALUMINATE (View Aspirin Dialuminate Review and Aspirin Dialuminate Label )
- NORVASC (View Norvasc Review and Norvasc Label )
Aggression, Suicide Attempt (8334843-9)
on Apr 23, 2012 Female patient from JAPAN , 39 years of age, was diagnosed with
- seasonal allergy
Patient was taking other medications:
- LITIOMAL (View Litiomal Review and Litiomal Label )
- CLONAZEPAM (View Clonazepam Review and Clonazepam Label )
- GOODMIN (View Goodmin Review and Goodmin Label )
- YAZ (1 Df, Qd) (View Yaz Review and Yaz Label )
- ETICALM (View Eticalm Review and Eticalm Label )
Juvenile Arthritis, Hepatic Function Abnormal (8323395-5)
on Apr 27, 2012 Female patient from JAPAN , weighting 103.6 lb, was diagnosed with
- rhinitis allergic
Patient was taking other medications:
- METHOTREXATE (View Methotrexate Review and Methotrexate Label )
- FOLIC ACID (View Folic Acid Review and Folic Acid Label )
- PREDNISOLONE (View Prednisolone Review and Prednisolone Label )
Haematocrit Increased, Leukocytosis, Chronic Myeloid Leukaemia (8125354-4)
Patient was taking Olopatadine Hcl (View Usage). After Olopatadine was administered, patient had the following side effects: haematocrit increased, leukocytosis, chronic myeloid leukaemia on Jan 30, 2012 from JAPAN Additional patient health information: Male patient , weighting 211.6 lb, was diagnosed with
- rhinitis allergic
- gastrooesophageal reflux disease
- right ventricular failure
Patient was taking other medications:
- RABEPRAZOLE SODIUM (10mg Per Day) (View Rabeprazole Sodium Review and Rabeprazole Sodium Label )
- TORSEMIDE (8mg Per Day) (View Torsemide Review and Torsemide Label )
- LISINOPRIL (10mg Per Day) (View Lisinopril Review and Lisinopril Label )
- ETHYL ICOSAPENTATE (1800mg Per Day) (View Ethyl Icosapentate Review and Ethyl Icosapentate Label )
- ALLOPURINOL (100mg Per Day) (View Allopurinol Review and Allopurinol Label )
- FLOLAN (View Flolan Review and Flolan Label )
Loss Of Consciousness, Nausea (8105502-2)
Adverse event was reported on Jan 30, 2012 by a Female patient taking Olopatadine Hcl (View Usage) (Dosage: 10 Mg, 1x/day) . Location: JAPAN , 69 years of age, Patient experienced the following unwanted or unexpected effects: loss of consciousness, nausea (nausea Questions).
Patient was taking other medications:
- LYRICA (50 Mg, 2x/day) (View Lyrica Review and Lyrica Label )
- MUCODYNE (1000 Mg, 1x/day) (View Mucodyne Review and Mucodyne Label )
- CLEANAL (400 Mg, 1x/day) (View Cleanal Review and Cleanal Label )
Hepatic Neoplasm Malignant, Pyrexia, Neutrophil Count Increased, Hepatic Function Abnormal, Insomnia, Hypertension, Constipation (8065380-7)
on Jan 20, 2012 Male patient from JAPAN , 54 years of age, weighting 138.9 lb, was treated with Olopatadine Hcl (View Usage). Patient had the following side effects: hepatic neoplasm malignant, pyrexia, neutrophil count increased, hepatic function abnormal, insomnia, hypertension, constipation (constipation Questions). Olopatadine Hcl dosage: Daily Dose 10 Mg.
Patient was taking other medications:
- ATARAX (Daily Dose 50 Mg) (View Atarax Review and Atarax Label )
- NEXAVAR (400 Mg, Qd) (View Nexavar Review and Nexavar Label )
- LANSOPRAZOLE (Daily Dose 15 Mg) (View Lansoprazole Review and Lansoprazole Label )
- HIRUDOID (Unk) (View Hirudoid Review and Hirudoid Label )
Blood Glucose Increased (8029858-4)
on Dec 27, 2011 Male patient from JAPAN , 73 years of age, weighting 154.3 lb, was treated with Olopatadine Hcl(View Usage). After Olopatadine was administered, patient had the following side effects: blood glucose increased. Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
- ANTITHROMBOTIC AGENTS (View Antithrombotic Agents Review and Antithrombotic Agents Label )
- CONIEL (View Coniel Review and Coniel Label )
- PLAVIX (View Plavix Review and Plavix Label )
- ANPLAG (View Anplag Review and Anplag Label )
- ASPIRIN (View Aspirin Review and Aspirin Label )
- BASEN (View Basen Review and Basen Label )
Blood Albumin Decreased, Aspartate Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Epstein-barr Virus Antibody Positive, Faeces Pale, Allergic Hepatitis, Prothrombin Time Prolonged, Malaise, Prothrombin Time Ratio Decreased (8018605-8)
Patient was taking Olopatadine Hcl (View Usage). Patient experienced the following unwanted or unexpected effects: blood albumin decreased, aspartate aminotransferase increased, blood lactate dehydrogenase increased, epstein-barr virus antibody positive, faeces pale, allergic hepatitis, prothrombin time prolonged, malaise, prothrombin time ratio decreased on Dec 20, 2011 from JAPAN Additional patient health information: Female patient , 81 years of age, was diagnosed with
- pruritus
Patient was taking other medications:
- ATARAX (View Atarax Review and Atarax Label )
- XYZAL (View Xyzal Review and Xyzal Label )
- CELESTAMINE TAB (View Celestamine Tab Review and Celestamine Tab Label )
Laceration (8007206-3)
Adverse event was reported on Dec 13, 2011 by a Female patient taking Olopatadine Hcl (View Usage) (Dosage: 5 Mg, 2x/day) was diagnosed with
- pruritus
Patient was taking other medications:
- HIRUDOID (Unk) (View Hirudoid Review and Hirudoid Label )
- DRENISON (Unk) (View Drenison Review and Drenison Label )
- LIPITOR (10 Mg, Uid/qd) (View Lipitor Review and Lipitor Label )
Pain, Myocardial Infarction, Cerebrovascular Accident, Pulmonary Embolism, Anxiety, Gallbladder Disorder, Deep Vein Thrombosis, Cholecystitis Acute, Cholecystitis Chronic (7912392-7)
on Nov 04, 2011 Female patient from UNITED STATES , 25 years of age, weighting 135.0 lb, was treated with Olopatadine Hydrochloride (View Usage). After Olopatadine was administered, patient had the following side effects: pain (pain Questions), myocardial infarction, cerebrovascular accident, pulmonary embolism (pulmonary embolism Questions), anxiety (anxiety Questions), gallbladder disorder, deep vein thrombosis (deep vein thrombosis Questions), cholecystitis acute, cholecystitis chronic. Olopatadine Hydrochloride dosage: Unk Unk, Prn.
Patient was taking other medications:
- XANAX (Unk) (View Xanax Review and Xanax Label )
- DROSPIRENONE AND ETHINYL ESTRADIOL (Unk) (View Drospirenone And Ethinyl Estradiol Review and Drospirenone And Ethinyl Estradiol Label )
- PREDNISONE (Unk) (View Prednisone Review and Prednisone Label )
- PEPCID (Unk Unk, Qd) (View Pepcid Review and Pepcid Label )
- YASMIN (Unk) (View Yasmin Review and Yasmin Label )
- ADVAIR DISKUS 100/50 (Unk) (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label )
- ALLEGRA (View Allegra Review and Allegra Label )
- FLONASE (View Flonase Review and Flonase Label )
Dyspnoea, Burning Sensation (7850789-4)
on Oct 19, 2011 Male patient from UNITED STATES , weighting 195.2 lb, was diagnosed with
- hypersensitivity
Patient was taking other medications:
- FLUTICASONE PROPIONATE (View Fluticasone Propionate Review and Fluticasone Propionate Label )
- PROAIR HFA (View Proair Hfa Review and Proair Hfa Label )
Pulmonary Artery Thrombosis, Venous Thrombosis (7833499-9)
Patient was taking Olopatadine Hcl (View Usage). Patient had the following side effects: pulmonary artery thrombosis, venous thrombosis on Oct 12, 2011 from JAPAN Additional patient health information: Female patient , 29 years of age, weighting 132.3 lb, was diagnosed with
- pruritus
- non-small cell lung cancer
- constipation (constipation Questions)
Patient was taking other medications:
- CRIZOTINIB (250 Mg, 2x/day) (View Crizotinib Review and Crizotinib Label )
- MILMAG (2 Tablets, As Needed) (View Milmag Review and Milmag Label )
- KINDAVATE (As Needed) (View Kindavate Review and Kindavate Label )
Jaw Disorder, Paralysis, Viith Nerve Paralysis, Apraxia, Tenderness, Cranial Nerve Palsies Multiple, Temporomandibular Joint Syndrome, Dysphagia, Trismus (7817466-7)
Adverse event was reported on Oct 03, 2011 by a Male patient taking Olopatadine Hcl (View Usage) (Dosage: N/A) . Location: JAPAN , 75 years of age, After Olopatadine was administered, patient had the following side effects: jaw disorder, paralysis (paralysis Questions), viith nerve paralysis, apraxia, tenderness, cranial nerve palsies multiple, temporomandibular joint syndrome, dysphagia, trismus.
Patient was taking other medications:
- MUCOSTA (View Mucosta Review and Mucosta Label )
- CEFAZOLIN SODIUM (Dosage Form: Powder) (View Cefazolin Sodium Review and Cefazolin Sodium Label )
- METHADERM (View Methaderm Review and Methaderm Label )
- FERRUM (View Ferrum Review and Ferrum Label )
- XYZAL (View Xyzal Review and Xyzal Label )
- TRANEXAMIC ACID (View Tranexamic Acid Review and Tranexamic Acid Label )
Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Hepatic Function Abnormal (7814212-8)
on Oct 04, 2011 Male patient from JAPAN , 71 years of age, weighting 160.9 lb, was treated with Olopatadine Hcl (View Usage). Patient experienced the following unwanted or unexpected effects: aspartate aminotransferase increased, alanine aminotransferase increased, hepatic function abnormal. Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
- ALLOPURINOL (View Allopurinol Review and Allopurinol Label )
- ARAVA (View Arava Review and Arava Label )
- URALYT (View Uralyt Review and Uralyt Label )
- AZULFIDINE (View Azulfidine Review and Azulfidine Label )
- FLIVAS (View Flivas Review and Flivas Label )
- S. ADCHNON (View S. Adchnon Review and S. Adchnon Label )
- COMELIAN (View Comelian Review and Comelian Label )
White Blood Cell Count Increased, Haematocrit Increased (7802479-1)
on Sep 29, 2011 Male patient from JAPAN , weighting 211.6 lb, was diagnosed with
- rhinitis allergic
- pulmonary arterial hypertension
- hyperuricaemia
- right ventricular failure
- dyslipidaemia
Patient was taking other medications:
- FLOLAN (View Flolan Review and Flolan Label )
- ALLOPURINOL (100mg Per Day) (View Allopurinol Review and Allopurinol Label )
- TORSEMIDE (8mg Per Day) (View Torsemide Review and Torsemide Label )
- ETHYL ICOSAPENTATE (1800mg Per Day) (View Ethyl Icosapentate Review and Ethyl Icosapentate Label )
- LISINOPRIL (10mg Per Day) (View Lisinopril Review and Lisinopril Label )
- RABEPRAZOLE SODIUM (10mg Per Day) (View Rabeprazole Sodium Review and Rabeprazole Sodium Label )
Thyroid Cancer (7777138-4)
Patient was taking Olopatadine Hcl (View Usage). After Olopatadine was administered, patient had the following side effects: thyroid cancer (thyroid cancer Questions) on Sep 13, 2011 from JAPAN Additional patient health information: Female patient , 37 years of age, weighting 179.0 lb, . Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
- SOLOSTAR (View Solostar Review and Solostar Label )
- METFORMIN HYDROCHLORIDE (2 Tab Each After Breakfast And Supper) (View Metformin Hydrochloride Review and Metformin Hydrochloride Label )
- LANTUS (View Lantus Review and Lantus Label )
Dermatitis Bullous (7704364-2)
Adverse event was reported on Aug 15, 2011 by a Female patient taking Olopatadine Hcl (View Usage) (Dosage: N/A) was diagnosed with
- hypersensitivity
- hypertension
Patient was taking other medications:
- COZAAR (View Cozaar Review and Cozaar Label )
- CARVEDILOL (View Carvedilol Review and Carvedilol Label )
- MUCOSTA (View Mucosta Review and Mucosta Label )
Thrombotic Cerebral Infarction, Decreased Appetite (7585927-4)
on Jun 20, 2011 Female patient from JAPAN , 77 years of age, weighting 108.0 lb, was diagnosed with
- pruritus
Patient was taking other medications:
- VICTOZA (0.6 Mg, Qd) (View Victoza Review and Victoza Label )
Aspartate Aminotransferase Increased, Hypersensitivity, Alanine Aminotransferase Increased, Eczema Asteatotic, Lymphocyte Count Decreased, Blood Amylase Increased, Rash, Blood Creatinine Increased (7561801-4)
on Jun 14, 2011 Male patient from JAPAN , weighting 121.3 lb, was treated with Olopatadine(View Usage). After Olopatadine was administered, patient had the following side effects: aspartate aminotransferase increased, hypersensitivity, alanine aminotransferase increased, eczema asteatotic, lymphocyte count decreased, blood amylase increased, rash (rash Questions), blood creatinine increased. Olopatadine dosage: N/A.
Patient was taking other medications:
- GRANISETRON HCL (View Granisetron Hcl Review and Granisetron Hcl Label )
- PREDNISOLONE (View Prednisolone Review and Prednisolone Label )
- LEVOFLOXACIN (View Levofloxacin Review and Levofloxacin Label )
- FAMOTIDINE (View Famotidine Review and Famotidine Label )
- BENDAMUSTINE HCL (View Bendamustine Hcl Review and Bendamustine Hcl Label )
- DIFLUPREDNATE (View Difluprednate Review and Difluprednate Label )
- BROTIZOLAM (View Brotizolam Review and Brotizolam Label )
Hepatitis Acute (7554037-4)
Patient was taking Olopatadine Hcl (View Usage). Patient experienced the following unwanted or unexpected effects: hepatitis acute on Jun 14, 2011 from JAPAN Additional patient health information: Male patient , 22 years of age, . Olopatadine Hcl dosage: N/A.
Patient was taking other medications:
- ALLEGRA (View Allegra Review and Allegra Label )
Product Formulation Issue, Bone Pain, Asthenia, Viral Infection (7357691-5)
Adverse event was reported on Jul 14, 2010 by a Male patient taking Olopatadine (View Usage) (Dosage: N/A) . Location: UNITED STATES , 54 years of age, Patient had the following side effects: product formulation issue, bone pain, asthenia, viral infection (viral infection Questions).
Patient was taking other medications:
- ASPIRIN (View Aspirin Review and Aspirin Label )
- LASIX (View Lasix Review and Lasix Label )
- PROLASTIN C (5900 Mg, Qw, Iv) (View Prolastin-c Review and Prolastin-c Label )
White Blood Cell Count Increased, Pain Of Skin, Pyrexia, Mobility Decreased, Arthralgia, Hyperuricaemia, C-reactive Protein Increased, Erythrodermic Psoriasis (7315620-4)
on Feb 23, 2011 Male patient from JAPAN , 51 years of age, weighting 187.4 lb, was diagnosed with
- dermatitis exfoliative
- reflux oesophagitis
- hypertension
Patient was taking other medications:
- LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label )
- ENALAPRIL MALEATE (View Enalapril Maleate Review and Enalapril Maleate Label )
- WHITE PETROLEUM (Qs) (View White Petroleum Review and White Petroleum Label )
- CARVEDILOL (View Carvedilol Review and Carvedilol Label )
- HEPARIN (Qs) (View Heparin Review and Heparin Label )
- METENOLONE (View Metenolone Review and Metenolone Label )
- BETAMETHASONE SODIUM PHOSPHATE (Qs) (View Betamethasone Sodium Phosphate Review and Betamethasone Sodium Phosphate Label )
- OFLOXACIN (Qs) (View Ofloxacin Review and Ofloxacin Label )
Breast Cancer (6085275-8)
on Jan 05, 2008 Male patient from UNITED STATES , 88 years of age, weighting 160.0 lb, was diagnosed with
- nasal congestion
Patient was taking other medications:
- PLAVIX (View Plavix Review and Plavix Label )
- OMEPRAZOLE (View Omeprazole Review and Omeprazole Label )
- GLYBURIDE (View Glyburide Review and Glyburide Label )
- LISINOPRIL (View Lisinopril Review and Lisinopril Label )
- ATENOLOL (View Atenolol Review and Atenolol Label )
- DILANTIN (View Dilantin Review and Dilantin Label )
- SIMVASTATIN (View Simvastatin Review and Simvastatin Label )
- LORATADINE (View Loratadine Review and Loratadine Label )
Showing 1-25 of 27 Next Page >
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Olopatadine InformationAlternative OLOPATADINE Names:OLOPATADI Substance:OLOPATADI Side Effects reported to FDA: 27. View FDA Adverse Reports Olopatadine safety alerts: No Reported deaths: 2 Reported hospitalizations: 12 |
Olopatadine Side Effects