CORNEAL LESION side effect
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Zoloft Side Effects Report #5664945-7
Consumer or non-health professional from ARGENTINA reported ZOLOFT problem on Mar 05, 2008. Female patient, weighting 134.5 lb, was diagnosed with depression and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: corneal lesion, dry eye, dry skin, hyperhidrosis, . ZOLOFT dosage: unknown. During the same period patient was treated with CLONAZEPAM. Patient recovered.
Zoloft Side Effects Report #5685209-1
ZOLOFT problem was reported by a Consumer or non-health professional from ARGENTINA on Mar 17, 2008. Female patient, weighting 134.5 lb, was diagnosed with depression and was treated with ZOLOFT. After drug was administered, patient experienced the following problems/side effects: corneal lesion, dry eye, dry skin, hyperhidrosis, . ZOLOFT dosage: unknown. During the same period patient was treated with CLONAZEPAM. Patient recovered.
Lamictal Side Effects Report #5393863-7
Pharmacist from FRANCE reported LAMICTAL problem on July 16, 2007. Female patient, 53 years of age, weighting 132.3 lb, was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: corneal lesion, dry eye, eye irritation, off label use, visual acuity reduced, . LAMICTAL dosage: unknown. During the same period patient was treated with LAROXYL, PROPOFOL, SKENAN. Patient was hospitalized and became disabled. Patient recovered.
Neoral Side Effects Report #5401164-3
NEORAL problem was reported by a Pharmacist from NETHERLANDS on July 23, 2007. Female patient, 54 years of age, was diagnosed with psoriasis and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: corneal lesion, visual acuity reduced, . NEORAL dosage: 125 MG, BID. During the same period patient was treated with METHOTREXATE, DOVOBET, DERMOVATE, PROTOPIC. Patient recovered.
Lamictal Side Effects Report #5393863-7
Pharmacist from FRANCE reported LAMICTAL problem on July 16, 2007. Female patient, 53 years of age, weighting 132.3 lb, was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: corneal lesion, dry eye, eye irritation, off label use, visual acuity reduced, . LAMICTAL dosage: unknown. During the same period patient was treated with LAROXYL, PROPOFOL, SKENAN. Patient was hospitalized and became disabled. Patient recovered.
Neoral Side Effects Report #5401164-3
NEORAL problem was reported by a Pharmacist from NETHERLANDS on July 23, 2007. Female patient, 54 years of age, was diagnosed with psoriasis and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: corneal lesion, visual acuity reduced, . NEORAL dosage: 125 MG, BID. During the same period patient was treated with METHOTREXATE, DOVOBET, DERMOVATE, PROTOPIC. Patient recovered.
Alimta Side Effects Report #5780470-7
Physician from FRANCE reported ALIMTA problem on June 10, 2008. Female patient, 60 years of age, was diagnosed with non-small cell lung cancer, vitamin supplementation, prophylaxis and was treated with ALIMTA. After drug was administered, patient experienced the following problems/side effects: corneal lesion, uveitis, . ALIMTA dosage: 500 MG/M2, EVERY 3 WEEKS. During the same period patient was treated with FOLIC ACID, VITAMIN B, FLECAINIDE ACETATE. Patient recovered.
Lamictal Side Effects Report #5373546-X
LAMICTAL problem was reported by a Pharmacist from FRANCE on June 18, 2007. Female patient, 53 years of age, was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: corneal lesion, eye irritation, off label use, . LAMICTAL dosage: unknown. Patient recovered.
Orfadin Side Effects Report #5327599-5
Consumer or non-health professional from UNITED STATES reported ORFADIN problem on Aug 28, 2006. Male patient was diagnosed with alkaptonuria and was treated with ORFADIN. After drug was administered, patient experienced the following problems/side effects: corneal lesion, corneal opacity, eye pain, pinguecula, . ORFADIN dosage: 2 MILLIGRAM A DAY ORAL. Patient recovered.
Neoral Side Effects Report #5465248-6
NEORAL problem was reported by a Pharmacist from NETHERLANDS on Sept 13, 2007. Female patient, 54 years of age, was diagnosed with psoriasis and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: corneal dystrophy, corneal lesion, keratitis, visual acuity reduced, . NEORAL dosage: 125 MG, BID. During the same period patient was treated with METHOTREXATE, DOVOBET, DERMOVATE, PROTOPIC. Patient recovered.
Neoral Side Effects Report #5440789-6
Pharmacist from NETHERLANDS reported NEORAL problem on Aug 27, 2007. Female patient, 54 years of age, was diagnosed with psoriasis and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: corneal dystrophy, corneal lesion, keratitis, visual acuity reduced, . NEORAL dosage: 125 MG, BID. During the same period patient was treated with METHOTREXATE, DOVOBET, DERMOVATE, PROTOPIC. Patient recovered.
Sandimmune Side Effects Report #5727267-1
SANDIMMUNE problem was reported by a Consumer or non-health professional from NORWAY on Apr 23, 2008. Male patient, 28 years of age, was diagnosed with transplant and was treated with SANDIMMUNE. After drug was administered, patient experienced the following problems/side effects: cataract, corneal lesion, retinal depigmentation, schimke immunoosseous dysplasia, . SANDIMMUNE dosage: 75 MG, BID. During the same period patient was treated with PREDNISOLONE. Patient recovered.
Sandimmune Side Effects Report #5717267-X
Consumer or non-health professional from reported SANDIMMUNE problem on Apr 23, 2008. Male patient, 28 years of age, was diagnosed with transplant and was treated with SANDIMMUNE. After drug was administered, patient experienced the following problems/side effects: cataract, corneal lesion, retinal depigmentation, schimke immunoosseous dysplasia, . SANDIMMUNE dosage: 75 MG, BID. During the same period patient was treated with PREDNISOLONE. Patient recovered.
Sandimmune Side Effects Report #5723422-5
SANDIMMUNE problem was reported by a Consumer or non-health professional from NORWAY on Apr 23, 2008. Male patient, 28 years of age, was diagnosed with transplant and was treated with SANDIMMUNE. After drug was administered, patient experienced the following problems/side effects: cataract, corneal lesion, retinal depigmentation, schimke immunoosseous dysplasia, . SANDIMMUNE dosage: 75 MG, BID. During the same period patient was treated with PREDNISOLONE. Patient recovered.