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Cialis Side Effects Report #5646906-7
Physician from FRANCE reported CIALIS problem on Feb 22, 2008. Male patient, 55 years of age, was diagnosed with erectile dysfunction and was treated with CIALIS. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, flushing, gastrooesophageal reflux disease, nasal congestion, ventricular extrasystoles, . CIALIS dosage: 10 MG, WEEKLY (1/W). Patient recovered.

Avelox Side Effects Report #5652473-4
AVELOX problem was reported by a Physician from JAPAN on Feb 22, 2008. Male patient, 55 years of age, weighting 145.5 lb, was diagnosed with nasopharyngitis and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, diarrhoea, hepatic function abnormal, lip swelling, oral mucosa erosion, pain in extremity, pyrexia, stevens-johnson syndrome, . AVELOX dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 400 MG. During the same period patient was treated with LOXONIN, MUCOSTA. Patient was hospitalized. Patient recovered.

Albendazole Side Effects Report #5679012-6
Physician from GHANA reported ALBENDAZOLE problem on Mar 18, 2008. Female patient, 64 years of age, weighting 328.5 lb, was diagnosed with filariasis lymphatic and was treated with ALBENDAZOLE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, dermatitis exfoliative, oedema peripheral, oral pain, palpitations, pitting oedema, rash, stevens-johnson syndrome, . ALBENDAZOLE dosage: unknown. During the same period patient was treated with MECTIZAN. Patient was hospitalized. Patient recovered.

Stromectol Side Effects Report #5679130-2
STROMECTOL problem was reported by a Physician from GHANA on Mar 18, 2008. Female patient, 64 years of age, was diagnosed with filariasis lymphatic and was treated with STROMECTOL. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, dermatitis exfoliative, oedema peripheral, oral pain, palpitations, pitting oedema, rash, stevens-johnson syndrome, . STROMECTOL dosage: unknown. During the same period patient was treated with ALBENDAZOLE. Patient was hospitalized. Patient recovered.


Combigan Side Effects Report #5679825-0
Consumer or non-health professional from UNITED STATES reported COMBIGAN problem on Mar 18, 2008. Male patient was diagnosed with glaucoma and was treated with COMBIGAN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, entropion, ulcerative keratitis, . COMBIGAN dosage: unknown. During the same period patient was treated with LUMIGAN. Patient recovered.

Albendazole Side Effects Report #5680453-1
ALBENDAZOLE problem was reported by a Health Professional from GHANA on Mar 18, 2008. Female patient, 64 years of age, was treated with ALBENDAZOLE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, oedema peripheral, oral pain, palpitations, pruritus, rash, stevens-johnson syndrome, vision blurred, . ALBENDAZOLE dosage: unknown. During the same period patient was treated with MECTIZAN. Patient was hospitalized. Patient recovered.

Albendazole Side Effects Report #5682842-8
Physician from GHANA reported ALBENDAZOLE problem on Mar 18, 2008. Female patient, 64 years of age, was treated with ALBENDAZOLE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, dermatitis exfoliative, oedema peripheral, oral pain, palpitations, pitting oedema, rash, stevens-johnson syndrome, . ALBENDAZOLE dosage: unknown. During the same period patient was treated with MECTIZAN. Patient was hospitalized. Patient recovered.

Albendazole Side Effects Report #5682868-4
ALBENDAZOLE problem was reported by a Physician from GHANA on Mar 18, 2008. Female patient, 64 years of age, weighting 328.5 lb, was treated with ALBENDAZOLE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, dermatitis exfoliative, oedema peripheral, oral pain, palpitations, pitting oedema, rash, stevens-johnson syndrome, . ALBENDAZOLE dosage: unknown. During the same period patient was treated with MECTIZAN. Patient was hospitalized. Patient recovered.

Xalatan Side Effects Report #5683391-3
Physician from BOSNIA AND HERZEGOWINA reported XALATAN problem on Mar 19, 2008. Male patient, 59 years of age, weighting 220.5 lb, was diagnosed with intraocular pressure increased and was treated with XALATAN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, conjunctival oedema, eyelid oedema, hypersensitivity, . XALATAN dosage: unknown. During the same period patient was treated with TIMALEN, AZOPT. Patient recovered.


Tamiflu Side Effects Report #5612398-7
TAMIFLU problem was reported by a Health Professional from JAPAN on Jan 22, 2008. Male patient, 13 years of age, weighting 103.6 lb, was treated with TAMIFLU. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, mucosal erosion, oropharyngeal blistering, stevens-johnson syndrome, stomatitis, . TAMIFLU dosage: unknown. During the same period patient was treated with MUCODYNE, MIYA BM, CALONAL, AZITHROMYCIN HYDRATE, CLINDAMYCIN, METHYLPREDNISOLONE. Patient was hospitalized. Patient recovered.

Avelox Side Effects Report #5613664-1
Physician from JAPAN reported AVELOX problem on Jan 28, 2008. Male patient, 55 years of age, weighting 145.5 lb, was diagnosed with nasopharyngitis and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, diarrhoea, lip swelling, oral mucosal eruption, pain in extremity, pyrexia, swollen tongue, . AVELOX dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 400 MG. During the same period patient was treated with LOXONIN, MUCOSTA. Patient was hospitalized. Patient recovered.

Systane Side Effects Report #5619802-9
SYSTANE EYE DROPS problem was reported by a Health Professional from UNITED STATES on Jan 23, 2008. Female patient, 32 years of age, weighting 138.0 lb, was diagnosed with corneal abrasion, dry eye and was treated with SYSTANE EYE DROPS. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, conjunctival oedema, corneal erosion, eye burns, eye irritation, eye pain, lacrimation increased, no therapeutic response, . SYSTANE EYE DROPS dosage: unknown. During the same period patient was treated with SYSTANE EYE DROPS. Patient recovered.

Fluorometholone Side Effects Report #5623299-2
Physician from UNITED STATES reported FLUOROMETHOLONE problem on Feb 05, 2008. Male patient, 51 years of age, was diagnosed with episcleritis and was treated with FLUOROMETHOLONE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, eye pain, photophobia, scleral disorder, . FLUOROMETHOLONE dosage: unknown. Patient recovered.

Avelox Side Effects Report #5627296-2
AVELOX problem was reported by a Physician from JAPAN on Feb 05, 2008. Male patient, 55 years of age, weighting 145.5 lb, was diagnosed with nasopharyngitis and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, diarrhoea, lip swelling, oral mucosa erosion, pain in extremity, pyrexia, . AVELOX dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 400 MG. During the same period patient was treated with LOXONIN, MUCOSTA. Patient was hospitalized. Patient recovered.


Omniscan Side Effects Report #5642518-X
Physician from AUSTRIA reported OMNISCAN problem on Feb 16, 2008. Male patient, 53 years of age, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, nephrogenic systemic fibrosis, ocular icterus, . OMNISCAN dosage: unknown. During the same period patient was treated with ANGIOTENSIN CONVERTING ENZYME. Patient recovered.

Omniscan Side Effects Report #5642526-9
OMNISCAN problem was reported by a Physician from AUSTRIA on Feb 16, 2008. Female patient, 43 years of age, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, haemodialysis, metabolic acidosis, nephrogenic systemic fibrosis, ocular icterus, renal atrophy, . OMNISCAN dosage: unknown. During the same period patient was treated with ANGIOTENSIN II RECEPTOR BLOCKERS. Patient recovered.

Omniscan Side Effects Report #5642529-4
Physician from AUSTRIA reported OMNISCAN problem on Feb 16, 2008. Female patient, 52 years of age, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, myocardial infarction, nephrogenic systemic fibrosis, ocular icterus, . OMNISCAN dosage: unknown. During the same period patient was treated with ANGIOTENSIN II RECEPTOR BLOCKERS. Patient recovered.

Omniscan Side Effects Report #5642532-4
OMNISCAN problem was reported by a Physician from AUSTRIA on Feb 16, 2008. Female patient, 64 years of age, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, liver disorder, lung disorder, nephrogenic systemic fibrosis, ocular icterus, pain, pancreatic disorder, renal transplant, scleral disorder, . OMNISCAN dosage: unknown. During the same period patient was treated with ANGIOTENSIN II RECEPTOR BLOCKERS. Patient recovered.

Tamiflu Side Effects Report #5596068-X
Health Professional from JAPAN reported TAMIFLU problem on Jan 09, 2008. Male patient, 13 years of age, was treated with TAMIFLU. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, mucosal erosion, oropharyngeal blistering, stevens-johnson syndrome, stomatitis, . TAMIFLU dosage: unknown. During the same period patient was treated with ANTIBIOTIC NOS, ANALGESIC NOS, AZITHROMYCIN HYDRATE, CLINDAMYCIN, METHYLPREDNISOLONE. Patient was hospitalized. Patient recovered.


Augmentin Side Effects Report #5609717-4
AUGMENTIN problem was reported by a Consumer or non-health professional from SPAIN on Jan 25, 2008. Male patient, 40 years of age, was diagnosed with acute tonsillitis and was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, dysphonia, dyspnoea, laryngeal oedema, urticaria, . AUGMENTIN dosage: unknown. During the same period patient was treated with ENANTYUM. Patient recovered.

Cefzon Side Effects Report #5555427-1
Physician from JAPAN reported CEFZON problem on Dec 05, 2007. Male patient, weighting 144.0 lb, was diagnosed with gastroenteritis and was treated with CEFZON. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, oculomucocutaneous syndrome, stevens-johnson syndrome, . CEFZON dosage: unknown. During the same period patient was treated with LYSOZYME HYDROCHLORIDE, ALBUMIN TANNATE, LOPERAMIDE HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Cefzon Side Effects Report #5531229-7
CEFZON problem was reported by a Physician from JAPAN on Nov 21, 2007. Male patient, weighting 144.0 lb, was diagnosed with gastroenteritis and was treated with CEFZON. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, stevens-johnson syndrome, . CEFZON dosage: unknown. During the same period patient was treated with LYSOZYME HYDROCHLORIDE, ALBUMIN TANNATE, LOPERAMIDE HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Bss Side Effects Report #5480990-9
Physician from JAPAN reported BSS PLUS problem on Sept 20, 2007. Female patient, 73 years of age, was diagnosed with cataract operation and was treated with BSS PLUS. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, corneal oedema, corneal opacity, device malfunction, . BSS PLUS dosage: 400 ML; INTRAOCULAR. During the same period patient was treated with HEALON, BOSMIN, XYLOCAINE, BETAMETHASONE, TOBYRAMYCIN SULPHATE. Patient recovered.

Vesicare Side Effects Report #5483239-6
VESICARE problem was reported by a Physician from JAPAN on Sept 25, 2007. Female patient, 85 years of age, was diagnosed with hypertonic bladder, cerebral infarction, depression and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, parkinsonism, renal failure acute, rhabdomyolysis, . VESICARE dosage: 2.5 MG, ORAL; 2.5 MG, ORAL. During the same period patient was treated with GRAMILIL, PAXIL, BUFFERIN, EPADEL, IMPROMEN, ALFAROL, GEFANIL. Patient was hospitalized. Patient recovered.

Taxotere Side Effects Report #5483626-6
Health Professional from CANADA reported TAXOTERE problem on Oct 02, 2007. Female patient, 63 years of age, weighting 164.2 lb, was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, febrile neutropenia, photophobia, uveitis, vision blurred, . TAXOTERE dosage: unknown. During the same period patient was treated with MYCOSTATIN, PROCTOSEDYL, FLUCONAZOLE, DECADRON, ONDANSETRON, HYDROCORTISONE, NYSTATIN. Patient was hospitalized and became disabled. Patient recovered.

Taxotere Side Effects Report #5488061-2
TAXOTERE problem was reported by a Health Professional from CANADA on Oct 11, 2007. Female patient, 63 years of age, weighting 164.2 lb, was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, febrile neutropenia, photophobia, uveitis, vision blurred, . TAXOTERE dosage: unknown. During the same period patient was treated with MYCOSTATIN, PROCTOSEDYL, FLUCONAZOLE, DECADRON, ONDANSETRON, HYDROCORTISONE, NYSTATIN. Patient was hospitalized and became disabled. Patient recovered.

Velcade Side Effects Report #5500120-4
Physician from PORTUGAL reported VELCADE problem on Oct 15, 2007. Female patient, child -1 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, lacrimation increased, . VELCADE dosage: 1.30 MG/M2, INTRAVENOUS. Patient recovered.

Vesicare Side Effects Report #5453548-5
VESICARE problem was reported by a Physician from JAPAN on Sept 04, 2007. Female patient, 85 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, joint contracture, oral intake reduced, renal failure acute, rhabdomyolysis, tremor, white blood cell count increased, . VESICARE dosage: 2.5 MG, /D, ORAL. During the same period patient was treated with GRAMALIL, BUFFERIN, EPADEL, IMPROMEN, ALFAROL, GEFANIL, PURSENNID. Patient was hospitalized. Patient recovered.

Spiriva Side Effects Report #5460795-5
Consumer or non-health professional from UNITED STATES reported SPIRIVA problem on Sept 11, 2007. Female patient, 54 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, . SPIRIVA dosage: unknown. Patient recovered.

Nevirapine Side Effects Report #5406397-8
NEVIRAPINE problem was reported by a Consumer or non-health professional from on July 30, 2007. Male patient, 42 years of age, was diagnosed with hiv infection and was treated with NEVIRAPINE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, cutaneous leishmaniasis, hepatomegaly, immune reconstitution syndrome, rash, skin nodule, . NEVIRAPINE dosage: unknown. During the same period patient was treated with STAVUDINE, LAMIVUDINE. Patient recovered.

Vesicare Side Effects Report #5430341-0
Physician from JAPAN reported VESICARE problem on Aug 20, 2007. Female patient, 85 years of age, was diagnosed with hypertonic bladder and was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, depressed level of consciousness, joint contracture, renal failure acute, rhabdomyolysis, urinary retention, . VESICARE dosage: 2.5 MG, D, ORAL. During the same period patient was treated with GRAMALIL, BUFFERIN, EPADEL, IMPROMEN, ALFAROL, GEFANIL, PURSENNID. Patient was hospitalized. Patient recovered.

Botoxection Side Effects Report #5377736-1
BOTOXECTION problem was reported by a Physician from JAPAN on June 25, 2007. Female patient, 61 years of age, was diagnosed with blepharospasm and was treated with BOTOXECTION. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, corneal epithelium defect, corneal erosion, eye pain, keratitis, lagophthalmos, . BOTOXECTION dosage: unknown. Patient recovered.

Botoxection Side Effects Report #5377736-1
Physician from JAPAN reported BOTOXECTION problem on June 25, 2007. Female patient, 61 years of age, was diagnosed with blepharospasm and was treated with BOTOXECTION. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, corneal epithelium defect, corneal erosion, eye pain, keratitis, lagophthalmos, . BOTOXECTION dosage: unknown. Patient recovered.

Cefdinir Side Effects Report #5763309-5
CEFDINIR FINE GRANULE problem was reported by a Physician from JAPAN on May 30, 2008. Female patient, child 11 years of age, was diagnosed with upper respiratory tract inflammation and was treated with CEFDINIR FINE GRANULE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, corneal disorder, dysuria, oral mucosa erosion, pharyngeal erythema, stevens-johnson syndrome, . CEFDINIR FINE GRANULE dosage: unknown. During the same period patient was treated with PROCATEROL, CYPROHEPTADINE HYDROCHLORIDE, BROMHEXINE HYDROCHLORIDE, BECLOMETHASONE DIPROPIONATE. Patient was hospitalized. Patient recovered.

Atacand Side Effects Report #5779502-1
Consumer or non-health professional from UNITED STATES reported ATACAND problem on Sept 28, 2007. Male patient, 74 years of age, weighting 181.9 lb, was diagnosed with hypertension and was treated with ATACAND. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, cough, increased upper airway secretion, nasopharyngitis, . ATACAND dosage: unknown. Patient recovered.

Xalatan Side Effects Report #5729239-X
XALATAN problem was reported by a Physician from on Apr 30, 2008. Male patient, 59 years of age, weighting 220.5 lb, was diagnosed with intraocular pressure increased, open angle glaucoma and was treated with XALATAN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, conjunctival oedema, erythema of eyelid, eyelid oedema, eyelids pruritus, hypersensitivity, . XALATAN dosage: unknown. During the same period patient was treated with TIMALEN, AZOPT. Patient was hospitalized. Patient recovered.

Ultravist Side Effects Report #5741725-5
Health Professional from UNITED STATES reported ULTRAVIST problem on Jan 23, 2007. Male patient, 53 years of age, was diagnosed with computerised tomogram and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, eye irritation, . ULTRAVIST dosage: UNIT DOSE: 150 ML. Patient recovered.

Osteluc Side Effects Report #5691675-8
OSTELUC problem was reported by a Pharmacist from JAPAN on Mar 27, 2008. Female patient, 31 years of age, was diagnosed with tenosynovitis and was treated with OSTELUC. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, localised oedema, mucosal erosion, skin exfoliation, swelling face, . OSTELUC dosage: unknown. Patient was hospitalized. Patient recovered.

Osteluc Side Effects Report #5693806-2
Pharmacist from JAPAN reported OSTELUC problem on Mar 31, 2008. Female patient, 31 years of age, was diagnosed with tenosynovitis and was treated with OSTELUC. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, localised oedema, mucosal erosion, skin exfoliation, swelling face, . OSTELUC dosage: unknown. Patient was hospitalized. Patient recovered.

Xalatan Side Effects Report #5698240-7
XALATAN problem was reported by a Physician from BOSNIA AND HERZEGOWINA on Mar 28, 2008. Male patient, 59 years of age, weighting 220.5 lb, was diagnosed with intraocular pressure increased and was treated with XALATAN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, conjunctival oedema, erythema of eyelid, eyelid oedema, eyelids pruritus, hypersensitivity, . XALATAN dosage: unknown. During the same period patient was treated with TIMALEN, AZOPT. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5705127-X
Physician from SPAIN reported FOSAMAX problem on Apr 09, 2008. Female patient, 65 years of age, weighting 138.9 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, facial pain, photophobia, . FOSAMAX dosage: unknown. During the same period patient was treated with DURAPATITE, PAROXETINE HYDROCHLORIDE, ALPRAZOLAM, HYDROCHLOROTHIAZIDE AND TELMISARTAN. Patient recovered.

Augmentin Side Effects Report #5705731-9
AUGMENTIN problem was reported by a Consumer or non-health professional from FRANCE on Apr 04, 2008. Male patient, 62 years of age, was treated with AUGMENTIN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, dermatitis bullous, erythema multiforme, oral disorder, purpura, skin lesion, toxic skin eruption, . AUGMENTIN dosage: unknown. Patient was hospitalized. Patient recovered.

Osteluc Side Effects Report #5708003-1
Pharmacist from JAPAN reported OSTELUC problem on Apr 09, 2008. Female patient, 31 years of age, was diagnosed with tenosynovitis and was treated with OSTELUC. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, localised oedema, mucosal erosion, skin exfoliation, swelling face, . OSTELUC dosage: unknown. Patient was hospitalized. Patient recovered.

Immucyst Side Effects Report #5341858-1
IMMUCYST problem was reported by a Health Professional from JAPAN on May 25, 2007. Female patient, 91 years of age, was diagnosed with bladder cancer and was treated with IMMUCYST. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, eye discharge, eye inflammation, visual acuity reduced, . IMMUCYST dosage: unknown. Patient recovered.

Immucyst Side Effects Report #5343776-1
Health Professional from JAPAN reported IMMUCYST problem on May 25, 2007. Female patient, 91 years of age, was diagnosed with bladder cancer and was treated with IMMUCYST. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, eye discharge, eye inflammation, visual acuity reduced, . IMMUCYST dosage: unknown. Patient recovered.

Immucyst Side Effects Report #5345068-3
IMMUCYST problem was reported by a Health Professional from JAPAN on May 25, 2007. Female patient, 91 years of age, was diagnosed with bladder cancer and was treated with IMMUCYST. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, eye discharge, eye inflammation, visual acuity reduced, . IMMUCYST dosage: unknown. Patient recovered.

Xalatan Side Effects Report #5348182-1
Physician from POLAND reported XALATAN problem on May 28, 2007. Female patient, weighting 154.3 lb, was treated with XALATAN. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, conjunctival oedema, erythema of eyelid, eyelid oedema, eyelids pruritus, hypersensitivity, lacrimation increased, visual disturbance, . XALATAN dosage: unknown. During the same period patient was treated with ANTIHYPERTENSIVES. Patient recovered.

Timolol Side Effects Report #5353006-2
TIMOLOL MALEATE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on May 21, 2007. Male patient, 76 years of age, was diagnosed with glaucoma and was treated with TIMOLOL MALEATE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, conjunctival oedema, dermatitis, ectropion, erythema, eye irritation, eye pain, periorbital oedema, skin exfoliation, . TIMOLOL MALEATE dosage: unknown. During the same period patient was treated with BRIMONIDINE TARTRATE, DORZOLAMIDE, LATANOPROST. Patient was hospitalized. Patient recovered.

Viscotears Side Effects Report #5360623-2
Physician from ISRAEL reported VISCOTEARS problem on June 05, 2007. Female patient, 57 years of age, was treated with VISCOTEARS. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, punctate keratitis, visual acuity reduced, . VISCOTEARS dosage: unknown. During the same period patient was treated with GENTEAL. Patient recovered.

Viscotears Side Effects Report #5361572-6
VISCOTEARS problem was reported by a Physician from ISRAEL on June 05, 2007. Female patient, 57 years of age, was treated with VISCOTEARS. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, punctate keratitis, visual acuity reduced, . VISCOTEARS dosage: unknown. During the same period patient was treated with GENTEAL. Patient recovered.

Timolol Side Effects Report #5363356-1
Consumer or non-health professional from UNITED KINGDOM reported TIMOLOL MALEATE problem on June 04, 2007. Male patient, 76 years of age, was diagnosed with open angle glaucoma and was treated with TIMOLOL MALEATE. After drug was administered, patient experienced the following problems/side effects: conjunctival hyperaemia, conjunctival oedema, dermatitis, ectropion, erythema, eye irritation, eye pain, periorbital oedema, skin exfoliation, . TIMOLOL MALEATE dosage: unknown. During the same period patient was treated with BRIMONIDINE TARTRATE, DORZOLAMIDE, LANTANOPROST. Patient was hospitalized. Patient recovered.