Please choose an event type to view the corresponding MedsFacts report:

DRUG EXPOSURE DURING PREGNANCY ( 63 FDA reports)
PREGNANCY ( 48 FDA reports)
PSORIASIS ( 43 FDA reports)
DRUG INEFFECTIVE ( 36 FDA reports)
DRUG INTERACTION ( 33 FDA reports)
CONDITION AGGRAVATED ( 29 FDA reports)
PUSTULAR PSORIASIS ( 21 FDA reports)
NAUSEA ( 19 FDA reports)
DIZZINESS ( 17 FDA reports)
HEADACHE ( 17 FDA reports)
SKIN LESION ( 17 FDA reports)
PREGNANCY OF PARTNER ( 16 FDA reports)
T-CELL LYMPHOMA ( 16 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 15 FDA reports)
ALOPECIA ( 14 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 14 FDA reports)
ERYTHRODERMIC PSORIASIS ( 14 FDA reports)
FATIGUE ( 14 FDA reports)
PRURITUS ( 14 FDA reports)
ARTHRALGIA ( 13 FDA reports)
ASTHENIA ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 13 FDA reports)
PYREXIA ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
VOMITING ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 12 FDA reports)
PAIN ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
WEIGHT DECREASED ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
DERMATITIS EXFOLIATIVE ( 11 FDA reports)
LYMPHADENOPATHY ( 11 FDA reports)
NEOPLASM MALIGNANT ( 11 FDA reports)
OFF LABEL USE ( 11 FDA reports)
RASH ( 11 FDA reports)
BACK PAIN ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
DIARRHOEA ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
HYPOALBUMINAEMIA ( 10 FDA reports)
LEUKOPENIA ( 10 FDA reports)
LIVE BIRTH ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
NODULE ( 10 FDA reports)
SKIN ULCER ( 10 FDA reports)
CAESAREAN SECTION ( 9 FDA reports)
COLITIS ULCERATIVE ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
CUSHING'S SYNDROME ( 9 FDA reports)
DRUG ADMINISTRATION ERROR ( 9 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
MYALGIA ( 9 FDA reports)
MYCOSIS FUNGOIDES ( 9 FDA reports)
OEDEMA PERIPHERAL ( 9 FDA reports)
PNEUMONITIS ( 9 FDA reports)
SINUS BRADYCARDIA ( 9 FDA reports)
COMPLETED SUICIDE ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
MALAISE ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
MYOPATHY ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
SWELLING ( 8 FDA reports)
ABORTION INDUCED ( 7 FDA reports)
ADRENAL INSUFFICIENCY ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
CHEILITIS ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
EXOSTOSIS ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
HYPERCHOLESTEROLAEMIA ( 7 FDA reports)
HYPERKERATOSIS ( 7 FDA reports)
INJECTION SITE ERYTHEMA ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
TREMOR ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 6 FDA reports)
EXTRASKELETAL OSSIFICATION ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GASTROINTESTINAL DISORDER ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
MALIGNANT MELANOMA ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
ORGANISING PNEUMONIA ( 6 FDA reports)
PYOGENIC GRANULOMA ( 6 FDA reports)
T-CELL LYMPHOMA STAGE IV ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
URINARY INCONTINENCE ( 6 FDA reports)
VISUAL FIELD DEFECT ( 6 FDA reports)
ANOREXIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CALCINOSIS ( 5 FDA reports)
CAPILLARY LEAK SYNDROME ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
ENTHESOPATHY ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
INJECTION SITE OEDEMA ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 5 FDA reports)
MYOSITIS ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
PROSTATE CANCER ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
SKIN ATROPHY ( 5 FDA reports)
STAPHYLOCOCCAL INFECTION ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARTHRITIS ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 4 FDA reports)
BASAL CELL CARCINOMA ( 4 FDA reports)
BILIARY DILATATION ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD CULTURE POSITIVE ( 4 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 4 FDA reports)
BONE DENSITY DECREASED ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CONGENITAL ANOMALY ( 4 FDA reports)
DEATH ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE IRRITATION ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
ORTHOSTATIC HYPERTENSION ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PERIUMBILICAL ABSCESS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PSORIATIC ARTHROPATHY ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
SYNDESMOPHYTE ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ARTHRITIS BACTERIAL ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONJUNCTIVAL IRRITATION ( 3 FDA reports)
COUGH ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAIR COLOUR CHANGES ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
ICHTHYOSIS ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MANIA ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NAIL BED INFECTION ( 3 FDA reports)
NEOPLASM SKIN ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
ONYCHOCLASIS ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PREGNANCY TEST POSITIVE ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PROSTATE CANCER METASTATIC ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN REACTION ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
TRI-IODOTHYRONINE FREE DECREASED ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WOUND ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ADRENAL ADENOMA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
AMNIORRHEXIS ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BASILAR ARTERY OCCLUSION ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BLOOD 25-HYDROXYCHOLECALCIFEROL DECREASED ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BODY MASS INDEX INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BONE SCAN ABNORMAL ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISTRIBUTIVE SHOCK ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSLIPIDAEMIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR HAEMORRHAGE ( 2 FDA reports)
ECTROPION ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ENCEPHALOCELE ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FOETAL DISORDER ( 2 FDA reports)
GASTRIC HAEMORRHAGE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HODGKIN'S DISEASE STAGE II ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
KAPOSI'S SARCOMA ( 2 FDA reports)
KERATOACANTHOMA ( 2 FDA reports)
KERATOSIS FOLLICULAR ( 2 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 2 FDA reports)
LEUKOCYTURIA ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIMB DEFORMITY ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
MACROCYTOSIS ( 2 FDA reports)
MASS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGOCELE ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NAIL PIGMENTATION ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OPEN ANGLE GLAUCOMA ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
OSTEOCALCIN DECREASED ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PUBIC PAIN ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SIALOADENITIS ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN CHAPPED ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SPERM COUNT DECREASED ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SYNDACTYLY ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VITREOUS DETACHMENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
XANTHELASMA ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTED PREGNANCY ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ACANTHOMA ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACHROMOTRICHIA ACQUIRED ( 1 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALBINISM ( 1 FDA reports)
ALOPECIA TOTALIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAL INFECTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANODONTIA ( 1 FDA reports)
ANOMALY OF MIDDLE EAR CONGENITAL ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL DECREASED ( 1 FDA reports)
BLOOD 1,25-DIHYDROXYCHOLECALCIFEROL INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FOLLICLE STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BOWMAN'S MEMBRANE DISORDER ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBROVASCULAR STENOSIS ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CONGENITAL HAND MALFORMATION ( 1 FDA reports)
CONTRACTED BLADDER ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYST ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DELAYED MENARCHE ( 1 FDA reports)
DELAYED PUBERTY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECZEMA HERPETICUM ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FORCEPS DELIVERY ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HIV TEST FALSE POSITIVE ( 1 FDA reports)
HYPERADRENOCORTICISM ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTRICHOSIS ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INDUCED LABOUR ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KERATOPLASTY ( 1 FDA reports)
LENTIGO MALIGNA STAGE UNSPECIFIED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA RECURRENT ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASTITIS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROALBUMINURIA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOSITIS OSSIFICANS ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE I ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC NEOPLASM ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERTUSSIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITYRIASIS RUBRA PILARIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POSTOPERATIVE THROMBOSIS ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCOLLAGEN TYPE I C-TERMINAL PROPEPTIDE INCREASED ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PROCTOSTOMY ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDARTHROSIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL ADENOMA ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TESTICULAR SEMINOMA (PURE) STAGE I ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TRI-IODOTHYRONINE FREE INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TWIN PREGNANCY ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE CALCIUM DECREASED ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE PHOSPHATE INCREASED ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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