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Glucophage Side Effects Report #5636982-X
Consumer or non-health professional from UNITED STATES reported GLUCOPHAGE problem on Mar 19, 2007. Female patient, 45 years of age, was treated with GLUCOPHAGE. After drug was administered, patient experienced the following problems/side effects: nail disorder, paraesthesia, . GLUCOPHAGE dosage: unknown. Patient recovered.

Byetta Side Effects Report #5653983-6
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 01, 2007. Female patient, 49 years of age, weighting 203.0 lb, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: nail disorder, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN. Patient recovered.

Crestor Side Effects Report #5563419-1
Consumer or non-health professional from UNITED STATES reported CRESTOR problem on May 04, 2007. Female patient, 78 years of age, weighting 68.12 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: nail disorder, nail growth abnormal, . CRESTOR dosage: unknown. During the same period patient was treated with FOSINOPRIL, ATENOLOL, PLAVIX, ASPIRIN. Patient recovered.

Tykerb Side Effects Report #5566765-0
TYKERB problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 17, 2007. Female patient, 54 years of age, weighting 212.5 lb, was diagnosed with breast cancer and was treated with TYKERB. After drug was administered, patient experienced the following problems/side effects: nail disorder, psoriasis, skin chapped, . TYKERB dosage: unknown. During the same period patient was treated with XELODA, LASIX, NEURONTIN, VITAMIN B CAP, ALLEGRA, NEXIUM. Patient recovered.


Soriatane Side Effects Report #5600312-X
Pharmacist from UNITED STATES reported SORIATANE problem on May 03, 2007. Male patient, 59 years of age, was treated with SORIATANE. After drug was administered, patient experienced the following problems/side effects: nail disorder, . SORIATANE dosage: 10 MG;QD;PO. Patient recovered.

Byetta Side Effects Report #5577537-5
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 22, 2007. Female patient, 53 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: nail disorder, onychalgia, onychomadesis, . BYETTA dosage: unknown. Patient recovered.

Arimidex Side Effects Report #5472711-0
Consumer or non-health professional from UNITED STATES reported ARIMIDEX problem on Oct 16, 2006. Female patient, 71 years of age, was diagnosed with breast cancer and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: nail disorder, . ARIMIDEX dosage: unknown. Patient recovered.

Arimidex Side Effects Report #5472730-4
ARIMIDEX problem was reported by a Health Professional from UNITED STATES on Oct 17, 2006. Female patient, 62 years of age, was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: nail disorder, . ARIMIDEX dosage: unknown. During the same period patient was treated with FIBER SUPPLEMENT, AMBIEN. Patient recovered.

Metformin Side Effects Report #5456876-2
Consumer or non-health professional from UNITED STATES reported METFORMIN HYDROCHLORIDE problem on Sept 17, 2007. Female patient, weighting 195.0 lb, was diagnosed with diabetes mellitus and was treated with METFORMIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: nail disorder, . METFORMIN HYDROCHLORIDE dosage: unknown. During the same period patient was treated with SYNTHROID, HYDROCHLOROTHIAZIDE, METOPROLOL SUCCINATE, GEMFIBROZIL. Patient recovered.


Tykerb Side Effects Report #5422391-5
TYKERB problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 17, 2007. Female patient, 54 years of age, was diagnosed with breast cancer and was treated with TYKERB. After drug was administered, patient experienced the following problems/side effects: nail disorder, psoriasis, skin chapped, . TYKERB dosage: unknown. During the same period patient was treated with XELODA, LASIX, NEURONTIN, VITAMIN B CAP, ALLEGRA, NEXIUM. Patient recovered.

Sutent Side Effects Report #5441145-7
Consumer or non-health professional from reported SUTENT problem on Aug 21, 2007. Female patient, 57 years of age, weighting 138.9 lb, was diagnosed with uterine leiomyosarcoma and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: nail disorder, . SUTENT dosage: unknown. During the same period patient was treated with NIFEDIPINE, METOPROLOL SUCCINATE. Patient recovered.

Zemplar Side Effects Report #5756011-7
ZEMPLAR problem was reported by a Consumer or non-health professional from UNITED STATES on May 07, 2008. Female patient, weighting 118.1 lb, was diagnosed with vitamin supplementation, pain, depression, arthritis and was treated with ZEMPLAR. After drug was administered, patient experienced the following problems/side effects: nail disorder, onychoclasis, . ZEMPLAR dosage: unknown. During the same period patient was treated with LICRICA, ESTRADIOL, LIDOCAINE, SERTRALINE, HYDROXYCHLOROQUINE SULPHATE. Patient recovered.

Byetta Side Effects Report #5773940-9
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Jan 14, 2008. Female patient, 49 years of age, weighting 203.0 lb, was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: nail disorder, onychomadesis, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, LIPITOR, ALTACE, TOPROL. Patient recovered.

Herceptin Side Effects Report #5781047-X
HERCEPTIN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on June 05, 2008. Female patient was diagnosed with breast cancer metastatic and was treated with HERCEPTIN. After drug was administered, patient experienced the following problems/side effects: nail disorder, onychoclasis, . HERCEPTIN dosage: 6 MG/KG, UNK. Patient recovered.


Avelox Side Effects Report #5781649-0
Pharmacist from UNITED STATES reported AVELOX problem on May 21, 2008. Female patient, 65 years of age, was diagnosed with upper respiratory tract infection and was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: nail disorder, onychomadesis, . AVELOX dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 400 MG. During the same period patient was treated with SULFAMETHOXAZOLE AND TRIMETHOPRIM, AZITHROMYCIN. Patient recovered.

Avelox Side Effects Report #5702292-5
AVELOX problem was reported by a Pharmacist from UNITED STATES on Mar 11, 2008. Female patient was treated with AVELOX. After drug was administered, patient experienced the following problems/side effects: nail disorder, onychomadesis, . AVELOX dosage: TOTAL DAILY DOSE: 400 MG UNIT DOSE: 400 MG. Patient recovered.

Sensipar Side Effects Report #5719971-6
Physician from UNITED STATES reported SENSIPAR problem on Mar 27, 2007. Female patient, weighting 227.1 lb, was diagnosed with hyperparathyroidism secondary and was treated with SENSIPAR. After drug was administered, patient experienced the following problems/side effects: nail disorder, . SENSIPAR dosage: unknown. During the same period patient was treated with VENOFER, HECTORAL, VITAMIN D, EPOGEN, HUMALOG, NOVOLIN, INSULIN, RENAGEL. Patient recovered.

Combivir Side Effects Report #5368443-X
COMBIVIR problem was reported by a Physician from UNITED STATES on June 21, 2007. Male patient, 26 years of age, weighting 165.0 lb, was diagnosed with hiv infection and was treated with COMBIVIR. After drug was administered, patient experienced the following problems/side effects: nail disorder, nerve injury, scar, skin hyperpigmentation, stevens-johnson syndrome, tongue disorder, tooth decalcification, . COMBIVIR dosage: 150MG 2X DAILY PO. During the same period patient was treated with VIRAMUNE. Patient was hospitalized. Patient recovered.

Crestor Side Effects Report #5369321-2
Consumer or non-health professional from UNITED STATES reported CRESTOR problem on Mar 09, 2007. Female patient, 72 years of age, weighting 175.0 lb, was diagnosed with blood cholesterol increased, hypertension and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: nail disorder, nail growth abnormal, onychoclasis, . CRESTOR dosage: unknown. During the same period patient was treated with SYNTHROID. Patient recovered.


Avastin Side Effects Report #5317181-8
AVASTIN problem was reported by a Health Professional from UNITED STATES on Apr 27, 2007. Female patient, 50 years of age, was diagnosed with breast cancer metastatic and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: nail disorder, . AVASTIN dosage: 10 MG/KG, Q2W. Patient recovered.

Champix Side Effects Report #5285376-8
Physician from IRELAND reported CHAMPIX problem on Mar 22, 2007. Male patient, 40 years of age, was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: nail disorder, pneumonia, . CHAMPIX dosage: unknown. Patient was hospitalized. Patient recovered.

Alimta Side Effects Report #5228067-1
ALIMTA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 04, 2006. Female patient was diagnosed with non-small cell lung cancer stage iv and was treated with ALIMTA. After drug was administered, patient experienced the following problems/side effects: nail disorder, . ALIMTA dosage: unknown. During the same period patient was treated with FOLIC ACID, VITAMIN B12, DEXAMETHASONE. Patient recovered.

Xeloda Side Effects Report #5252954-1
Physician from GERMANY reported XELODA problem on Jan 09, 2007. Female patient, 70 years of age, weighting 154.3 lb, was treated with XELODA. After drug was administered, patient experienced the following problems/side effects: nail disorder, paralysis, . XELODA dosage: unknown. During the same period patient was treated with TAXOTERE. Patient was hospitalized. Patient recovered.

Spiriva Side Effects Report #5256521-5
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 10, 2006. Female patient was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: nail disorder, skin laceration, . SPIRIVA dosage: unknown. Patient recovered.

Tarceva Side Effects Report #5259352-5
Physician from GERMANY reported TARCEVA problem on Feb 16, 2007. Male patient, 64 years of age, was treated with TARCEVA. After drug was administered, patient experienced the following problems/side effects: nail disorder, skin fissures, . TARCEVA dosage: unknown. Patient recovered.

Iressa Side Effects Report #5263878-8
IRESSA problem was reported by a Physician from UNITED STATES on Nov 30, 2004. Female patient, 55 years of age, weighting 143.0 lb, was diagnosed with lung neoplasm malignant and was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: nail disorder, pain in extremity, skin lesion, . IRESSA dosage: 250 MG DAIILY PO. During the same period patient was treated with DURAGESIC, VICODIN, ATARAX. Patient recovered.

Iressa Side Effects Report #5265579-9
Health Professional from UNITED STATES reported IRESSA problem on Apr 20, 2004. Male patient was diagnosed with glioblastoma and was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: nail disorder, . IRESSA dosage: 250 MG QD PO. Patient recovered.

Iressa Side Effects Report #5269562-9
IRESSA problem was reported by a Physician from UNITED STATES on Oct 23, 2003. Female patient, 70 years of age, was treated with IRESSA. After drug was administered, patient experienced the following problems/side effects: nail disorder, . IRESSA dosage: 250 MG PO. Patient recovered.

Glucophage Side Effects Report #5636998-3
Consumer or non-health professional from UNITED STATES reported GLUCOPHAGE problem on Apr 24, 2007. Female patient, weighting 99.21 lb, was treated with GLUCOPHAGE. After drug was administered, patient experienced the following problems/side effects: nail discolouration, nail disorder, . GLUCOPHAGE dosage: unknown. During the same period patient was treated with ACCUPRIL, DYAZIDE, FOLIC ACID. Patient recovered.

Humira Side Effects Report #5594980-9
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 08, 2008. Female patient, weighting 140.1 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthropathy, nail disorder, onychomadesis, . HUMIRA dosage: unknown. During the same period patient was treated with ATENOLOL, MELOXICAM, HYDROCHLOROTHIAZIDE, SULFASALAZINE, HYDROXYCHLOROQUINE PHOSPHATE. Patient was hospitalized. Patient recovered.

Lamisil Side Effects Report #5563350-1
Physician from DENMARK reported LAMISIL problem on Dec 10, 2007. Female patient, weighting 143.3 lb, was diagnosed with onychomycosis and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: nail disorder, rash, rash pruritic, skin disorder, . LAMISIL dosage: 250 MG/DAY. Patient recovered.

Crestor Side Effects Report #5563457-9
CRESTOR problem was reported by a Consumer or non-health professional from UNITED STATES on May 15, 2007. Female patient, 60 years of age, weighting 382.1 lb, was diagnosed with dyslipidaemia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: energy increased, nail disorder, pollakiuria, . CRESTOR dosage: unknown. During the same period patient was treated with NABUMETONE, CLARITIN, ACCOLATE, AVANDIA, SYNTHROID, SULAR, BENICAR, TYLENOL. Patient recovered.

Arimidex Side Effects Report #5472605-0
Consumer or non-health professional from UNITED STATES reported ARIMIDEX problem on Oct 31, 2006. Female patient, 80 years of age, weighting 145.3 lb, was diagnosed with breast cancer and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: endometrial hypertrophy, nail disorder, . ARIMIDEX dosage: unknown. During the same period patient was treated with SYNTHROID, DOXEPIN, KLONOPIN, LISINOPRIL. Patient recovered.

Vytorin Side Effects Report #5495339-5
VYTORIN problem was reported by a Physician from UNITED STATES on Oct 15, 2007. Female patient, 80 years of age, weighting 110.2 lb, was diagnosed with hypercholesterolaemia and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: fracture, nail disorder, pelvic fracture, promotion of wound healing, road traffic accident, skin disorder, therapeutic response unexpected, thrombosis, . VYTORIN dosage: unknown. During the same period patient was treated with ATENOLOL, SYNTHROID, ASPIRIN. Patient was hospitalized. Patient recovered.

Vytorin Side Effects Report #5463852-2
Consumer or non-health professional from UNITED STATES reported VYTORIN problem on Sept 11, 2007. Female patient, 80 years of age, was diagnosed with hypercholesterolaemia and was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: fracture, nail disorder, pelvic fracture, promotion of wound healing, road traffic accident, skin disorder, therapeutic response unexpected, thrombosis, . VYTORIN dosage: unknown. During the same period patient was treated with ATENOLOL, SYNTHROID. Patient was hospitalized. Patient recovered.

Abraxane Side Effects Report #5424573-5
ABRAXANE problem was reported by a Physician from UNITED STATES on Aug 14, 2007. Female patient, 64 years of age, weighting 151.0 lb, was diagnosed with breast cancer metastatic and was treated with ABRAXANE. After drug was administered, patient experienced the following problems/side effects: haemorrhage, nail disorder, nail toxicity, onychalgia, purulence, . ABRAXANE dosage: 180 MG TOTAL DOSE (100 MG/M2,WEEKLY X 3 WEEKS THEN 1 WEEK REST). During the same period patient was treated with COUMADIN, LORTAB, KYTRIL, PHENERGAN, SYNTHROID. Patient recovered.

Sutent Side Effects Report #5377732-4
Consumer or non-health professional from UNITED STATES reported SUTENT problem on June 23, 2007. Male patient, weighting 170.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: myocardial ischaemia, nail disorder, silent myocardial infarction, . SUTENT dosage: unknown. During the same period patient was treated with GEFITINIB. Patient recovered.

Tykerb Side Effects Report #5380335-9
TYKERB problem was reported by a Consumer or non-health professional from UNITED STATES on June 01, 2007. Female patient, 63 years of age, weighting 125.2 lb, was diagnosed with breast cancer and was treated with TYKERB. After drug was administered, patient experienced the following problems/side effects: diarrhoea, nail disorder, nail infection, onychalgia, . TYKERB dosage: 1250MG PER DAY. During the same period patient was treated with XELODA, ADVAIR DISKUS. Patient recovered.

Sutent Side Effects Report #5377732-4
Consumer or non-health professional from UNITED STATES reported SUTENT problem on June 23, 2007. Male patient, weighting 170.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: myocardial ischaemia, nail disorder, silent myocardial infarction, . SUTENT dosage: unknown. During the same period patient was treated with GEFITINIB. Patient recovered.

Tykerb Side Effects Report #5380335-9
TYKERB problem was reported by a Consumer or non-health professional from UNITED STATES on June 01, 2007. Female patient, 63 years of age, weighting 125.2 lb, was diagnosed with breast cancer and was treated with TYKERB. After drug was administered, patient experienced the following problems/side effects: diarrhoea, nail disorder, nail infection, onychalgia, . TYKERB dosage: 1250MG PER DAY. During the same period patient was treated with XELODA, ADVAIR DISKUS. Patient recovered.

Torisel Side Effects Report #5792079-X
Health Professional from UNITED STATES reported TORISEL problem on May 15, 2008. Male patient, 68 years of age, was diagnosed with renal cell carcinoma and was treated with TORISEL. After drug was administered, patient experienced the following problems/side effects: nail discolouration, nail disorder, onychomycosis, . TORISEL dosage: unknown. Patient recovered.

Luvox Side Effects Report #5794578-3
LUVOX problem was reported by a Consumer or non-health professional from IRAN (ISLAMIC REPUBLIC OF) on June 10, 2008. Male patient, 27 years of age, was treated with LUVOX. After drug was administered, patient experienced the following problems/side effects: nail discolouration, nail disorder, . LUVOX dosage: (100 MG, 1 D), ORAL. During the same period patient was treated with OLANZAPINE. Patient recovered.

Diovan Side Effects Report #5726975-6
Consumer or non-health professional from UNITED STATES reported DIOVAN HCT problem on July 03, 2007. Female patient was diagnosed with hypertension and was treated with DIOVAN HCT. After drug was administered, patient experienced the following problems/side effects: eye swelling, nail disorder, oedema peripheral, pharyngolaryngeal pain, . DIOVAN HCT dosage: 160MG VAL/25MG HCT. Patient recovered.

Ixempra Side Effects Report #5737437-4
IXEMPRA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 03, 2008. Female patient, 61 years of age, was treated with IXEMPRA. After drug was administered, patient experienced the following problems/side effects: full blood count decreased, nail disorder, vein discolouration, . IXEMPRA dosage: unknown. Patient recovered.

Escitalopram Side Effects Report #5354483-3
Health Professional from UNITED KINGDOM reported ESCITALOPRAM OXALATE problem on May 23, 2007. Female patient, 41 years of age, weighting 127.9 lb, was diagnosed with depression and was treated with ESCITALOPRAM OXALATE. After drug was administered, patient experienced the following problems/side effects: alopecia, nail disorder, . ESCITALOPRAM OXALATE dosage: 15 MG QD PO. During the same period patient was treated with ESCITALOPRAM OXALATE. Patient recovered.

Taxotere Side Effects Report #5332073-6
TAXOTERE problem was reported by a Physician from AUSTRALIA on May 15, 2007. Female patient was diagnosed with breast cancer and was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: glossitis, nail disorder, neutrophil count increased, pneumocystis jiroveci pneumonia, pyrexia, . TAXOTERE dosage: unknown. Patient was hospitalized. Patient recovered.

Nexium Side Effects Report #5312389-X
Consumer or non-health professional from UNITED STATES reported NEXIUM problem on Dec 27, 2006. Female patient, 70 years of age, weighting 170.0 lb, was diagnosed with gastritis, dyspepsia, oesophagitis and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: alopecia, nail disorder, . NEXIUM dosage: unknown. During the same period patient was treated with FOSAMAX. Patient recovered.

Crestor Side Effects Report #5235894-3
CRESTOR problem was reported by a Consumer or non-health professional from UNITED STATES on June 26, 2006. Female patient, 77 years of age, weighting 105.0 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: myalgia, nail disorder, . CRESTOR dosage: 5 MG QD PO. During the same period patient was treated with ACTONEL, THYROID, ULTRAM, ACIPHEX, CALCIUM. Patient recovered.

Crestor Side Effects Report #5237168-3
Consumer or non-health professional from UNITED STATES reported CRESTOR problem on Apr 04, 2005. Female patient, 73 years of age, weighting 157.0 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: myalgia, nail disorder, . CRESTOR dosage: 10 MG PO. During the same period patient was treated with LOPID, MICARDIS. Patient recovered.

Crestor Side Effects Report #5240884-0
CRESTOR problem was reported by a Health Professional from UNITED STATES on June 16, 2005. Male patient, 25 years of age, weighting 200.0 lb, was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: alopecia, nail disorder, . CRESTOR dosage: 20 MG PO. Patient recovered.

Taxol Side Effects Report #5252335-0
Consumer or non-health professional from UNITED STATES reported TAXOL problem on May 30, 2006. Female patient, 64 years of age, weighting 169.8 lb, was diagnosed with ovarian cancer and was treated with TAXOL. After drug was administered, patient experienced the following problems/side effects: erythema, nail disorder, skin disorder, . TAXOL dosage: unknown. During the same period patient was treated with PRANDIN, SYNTHROID, COZAAR, LOMOTIL, LEXAPRO, ZOFRAN, ATIVAN. Patient recovered.