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

DYSPNOEA ( 55 FDA reports)
NAUSEA ( 53 FDA reports)
PAIN ( 52 FDA reports)
GLAUCOMA ( 51 FDA reports)
FALL ( 50 FDA reports)
OCULAR HYPERAEMIA ( 50 FDA reports)
PNEUMONIA ( 50 FDA reports)
BACK PAIN ( 48 FDA reports)
ANXIETY ( 47 FDA reports)
HYPOAESTHESIA ( 44 FDA reports)
OSTEOMYELITIS ( 43 FDA reports)
VOMITING ( 43 FDA reports)
ANAEMIA ( 42 FDA reports)
FATIGUE ( 42 FDA reports)
EYE IRRITATION ( 41 FDA reports)
TOOTHACHE ( 41 FDA reports)
VISUAL ACUITY REDUCED ( 40 FDA reports)
AZOTAEMIA ( 39 FDA reports)
PAIN IN EXTREMITY ( 39 FDA reports)
OSTEONECROSIS OF JAW ( 38 FDA reports)
CONFUSIONAL STATE ( 36 FDA reports)
OEDEMA PERIPHERAL ( 35 FDA reports)
SYNCOPE ( 34 FDA reports)
VISION BLURRED ( 33 FDA reports)
DIZZINESS ( 32 FDA reports)
OSTEOARTHRITIS ( 32 FDA reports)
SPINAL COLUMN INJURY ( 31 FDA reports)
VISUAL FIELD DEFECT ( 31 FDA reports)
ASTHENIA ( 30 FDA reports)
ATELECTASIS ( 30 FDA reports)
EYE PAIN ( 30 FDA reports)
PLEURAL EFFUSION ( 30 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 29 FDA reports)
SPINAL OSTEOARTHRITIS ( 29 FDA reports)
PHOTOPSIA ( 28 FDA reports)
ANHEDONIA ( 27 FDA reports)
DIARRHOEA ( 27 FDA reports)
HYPOKALAEMIA ( 27 FDA reports)
OSTEOPENIA ( 27 FDA reports)
VISUAL IMPAIRMENT ( 27 FDA reports)
BONE DISORDER ( 26 FDA reports)
INJURY ( 26 FDA reports)
INSOMNIA ( 26 FDA reports)
CONSTIPATION ( 25 FDA reports)
DEPRESSION ( 25 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 25 FDA reports)
THYROID NEOPLASM ( 25 FDA reports)
CATARACT OPERATION ( 24 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 24 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 24 FDA reports)
RENAL CYST ( 24 FDA reports)
RIB FRACTURE ( 24 FDA reports)
VITREOUS FLOATERS ( 24 FDA reports)
ABDOMINAL PAIN ( 23 FDA reports)
CHEST PAIN ( 23 FDA reports)
CONTUSION ( 23 FDA reports)
ERYTHEMA ( 23 FDA reports)
MYALGIA ( 22 FDA reports)
THROMBOSIS ( 22 FDA reports)
URINARY TRACT INFECTION ( 22 FDA reports)
ARTERIOSCLEROSIS ( 21 FDA reports)
DEHYDRATION ( 21 FDA reports)
SCOLIOSIS ( 21 FDA reports)
BRONCHITIS CHRONIC ( 20 FDA reports)
DIVERTICULUM INTESTINAL ( 20 FDA reports)
EMOTIONAL DISTRESS ( 20 FDA reports)
ORAL DISORDER ( 20 FDA reports)
ABDOMINAL PAIN UPPER ( 19 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 19 FDA reports)
CAROTID BRUIT ( 19 FDA reports)
CHOLECYSTITIS ( 19 FDA reports)
CHOLELITHIASIS ( 19 FDA reports)
DECREASED INTEREST ( 19 FDA reports)
DEFORMITY ( 19 FDA reports)
DIABETIC NEUROPATHY ( 19 FDA reports)
DRUG INEFFECTIVE ( 19 FDA reports)
EXOSTOSIS ( 19 FDA reports)
GALLBLADDER DISORDER ( 19 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 19 FDA reports)
GOITRE ( 19 FDA reports)
HEPATIC LESION ( 19 FDA reports)
HEPATITIS ( 19 FDA reports)
HYPOPHAGIA ( 19 FDA reports)
LIFE EXPECTANCY SHORTENED ( 19 FDA reports)
LIGAMENT SPRAIN ( 19 FDA reports)
LIMB INJURY ( 19 FDA reports)
LUNG INFILTRATION ( 19 FDA reports)
LUNG NEOPLASM ( 19 FDA reports)
MUCOSAL INFLAMMATION ( 19 FDA reports)
MUCOSAL ULCERATION ( 19 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 19 FDA reports)
OEDEMA ( 19 FDA reports)
ONYCHOCLASIS ( 19 FDA reports)
ONYCHOMYCOSIS ( 19 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 19 FDA reports)
PIGMENTATION DISORDER ( 19 FDA reports)
PULMONARY MASS ( 19 FDA reports)
RENAL DISORDER ( 19 FDA reports)
RETINAL HAEMORRHAGE ( 19 FDA reports)
STAPHYLOMA ( 19 FDA reports)
TRACHEAL DEVIATION ( 19 FDA reports)
VASODILATATION ( 19 FDA reports)
BLOOD IRON DECREASED ( 18 FDA reports)
CELLULITIS ( 18 FDA reports)
DEBRIDEMENT ( 18 FDA reports)
DEPRESSED MOOD ( 18 FDA reports)
DIABETIC RETINOPATHY ( 18 FDA reports)
GINGIVAL BLEEDING ( 18 FDA reports)
GINGIVAL SWELLING ( 18 FDA reports)
HYPERKERATOSIS ( 18 FDA reports)
INFLAMMATION ( 18 FDA reports)
LUNG CONSOLIDATION ( 18 FDA reports)
NEPHROGENIC ANAEMIA ( 18 FDA reports)
PAIN IN JAW ( 18 FDA reports)
PANCYTOPENIA ( 18 FDA reports)
RENAL FAILURE CHRONIC ( 18 FDA reports)
SERUM FERRITIN INCREASED ( 18 FDA reports)
SKIN ATROPHY ( 18 FDA reports)
SWELLING ( 18 FDA reports)
CATARACT ( 17 FDA reports)
DYSPHAGIA ( 17 FDA reports)
ESCHERICHIA INFECTION ( 17 FDA reports)
EYE SWELLING ( 17 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 17 FDA reports)
MUSCULAR WEAKNESS ( 17 FDA reports)
PRIMARY SEQUESTRUM ( 17 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
SKIN DISCOLOURATION ( 17 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 16 FDA reports)
CULTURE URINE POSITIVE ( 16 FDA reports)
DISABILITY ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
HYPERSENSITIVITY ( 16 FDA reports)
PARAESTHESIA ( 16 FDA reports)
STAPHYLOCOCCAL INFECTION ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
ARTHRALGIA ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
BRUXISM ( 15 FDA reports)
EAR PAIN ( 15 FDA reports)
FACIAL BONES FRACTURE ( 15 FDA reports)
HIP FRACTURE ( 15 FDA reports)
MENTAL STATUS CHANGES ( 15 FDA reports)
OSTEOMA ( 15 FDA reports)
PERIPHERAL COLDNESS ( 15 FDA reports)
THROMBOCYTOPENIA ( 15 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 14 FDA reports)
BONE FISSURE ( 14 FDA reports)
CARDIOMEGALY ( 14 FDA reports)
COLPOCELE ( 14 FDA reports)
DECUBITUS ULCER ( 14 FDA reports)
EYE PRURITUS ( 14 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 14 FDA reports)
GAIT DISTURBANCE ( 14 FDA reports)
HEARING IMPAIRED ( 14 FDA reports)
HERPES ZOSTER ( 14 FDA reports)
HYPOTHYROIDISM ( 14 FDA reports)
HYPOXIA ( 14 FDA reports)
KIDNEY SMALL ( 14 FDA reports)
LEUKOPENIA ( 14 FDA reports)
MULTIPLE FRACTURES ( 14 FDA reports)
NEURALGIA ( 14 FDA reports)
OSTEOLYSIS ( 14 FDA reports)
PROTEIN URINE ( 14 FDA reports)
SKIN ULCER ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
TOOTH EXTRACTION ( 14 FDA reports)
VAGINAL PROLAPSE ( 14 FDA reports)
VITAMIN D DEFICIENCY ( 14 FDA reports)
BLADDER DISORDER ( 13 FDA reports)
BLINDNESS ( 13 FDA reports)
BRONCHITIS ( 13 FDA reports)
CYSTOSCOPY ( 13 FDA reports)
FAECALOMA ( 13 FDA reports)
GANGRENE ( 13 FDA reports)
HYPERKALAEMIA ( 13 FDA reports)
HYPERLIPIDAEMIA ( 13 FDA reports)
IMPAIRED HEALING ( 13 FDA reports)
LUMBAR SPINAL STENOSIS ( 13 FDA reports)
MACULAR DEGENERATION ( 13 FDA reports)
MENTAL DISORDER ( 13 FDA reports)
PHOTOPHOBIA ( 13 FDA reports)
STRESS URINARY INCONTINENCE ( 13 FDA reports)
VARICOSE VEIN ( 13 FDA reports)
ARTHROPATHY ( 12 FDA reports)
BALANCE DISORDER ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 12 FDA reports)
DEAFNESS ( 12 FDA reports)
DIABETES MELLITUS ( 12 FDA reports)
HYPOVOLAEMIA ( 12 FDA reports)
INFECTED SKIN ULCER ( 12 FDA reports)
INTERMITTENT CLAUDICATION ( 12 FDA reports)
LACRIMATION INCREASED ( 12 FDA reports)
OSTEONECROSIS ( 12 FDA reports)
POST HERPETIC NEURALGIA ( 12 FDA reports)
PSYCHOTIC DISORDER ( 12 FDA reports)
ABSCESS DRAINAGE ( 11 FDA reports)
BLEPHARITIS ( 11 FDA reports)
CEREBRAL INFARCTION ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
DEEP VEIN THROMBOSIS ( 11 FDA reports)
HYPERTENSION ( 11 FDA reports)
METASTASES TO BONE ( 11 FDA reports)
NEUROPATHIC ULCER ( 11 FDA reports)
SINUSITIS ( 11 FDA reports)
SPINAL COLUMN STENOSIS ( 11 FDA reports)
SWELLING FACE ( 11 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 11 FDA reports)
ABSCESS ( 10 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
BONE CYST ( 10 FDA reports)
BONE LOSS ( 10 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 10 FDA reports)
BURSITIS ( 10 FDA reports)
CALCULUS URINARY ( 10 FDA reports)
CARDIOMYOPATHY ( 10 FDA reports)
CEREBRAL ATROPHY ( 10 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 10 FDA reports)
COLITIS ISCHAEMIC ( 10 FDA reports)
CORONARY ARTERY DISEASE ( 10 FDA reports)
DECREASED ACTIVITY ( 10 FDA reports)
DILATATION ATRIAL ( 10 FDA reports)
DYSAESTHESIA ( 10 FDA reports)
EJECTION FRACTION DECREASED ( 10 FDA reports)
ERYTHEMA OF EYELID ( 10 FDA reports)
GINGIVITIS ( 10 FDA reports)
HAEMORRHAGIC DIATHESIS ( 10 FDA reports)
HEART VALVE INCOMPETENCE ( 10 FDA reports)
HYPOCOAGULABLE STATE ( 10 FDA reports)
HYPOREFLEXIA ( 10 FDA reports)
JAW DISORDER ( 10 FDA reports)
JAW FRACTURE ( 10 FDA reports)
JOINT EFFUSION ( 10 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
MAJOR DEPRESSION ( 10 FDA reports)
MASTICATION DISORDER ( 10 FDA reports)
MENISCAL DEGENERATION ( 10 FDA reports)
MENISCUS LESION ( 10 FDA reports)
METASTATIC NEOPLASM ( 10 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 10 FDA reports)
OPEN REDUCTION OF FRACTURE ( 10 FDA reports)
OTITIS EXTERNA ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
PHYSICAL DISABILITY ( 10 FDA reports)
POLYMYALGIA RHEUMATICA ( 10 FDA reports)
POOR PERIPHERAL CIRCULATION ( 10 FDA reports)
POSTURE ABNORMAL ( 10 FDA reports)
ROTATOR CUFF SYNDROME ( 10 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 10 FDA reports)
SUICIDAL IDEATION ( 10 FDA reports)
THROMBOPHLEBITIS ( 10 FDA reports)
TOOTH IMPACTED ( 10 FDA reports)
URINARY INCONTINENCE ( 10 FDA reports)
VITREOUS DETACHMENT ( 10 FDA reports)
AGITATION ( 9 FDA reports)
BLADDER NECK OPERATION ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
CORNEAL OPERATION ( 9 FDA reports)
CYSTOPEXY ( 9 FDA reports)
DRUG INTOLERANCE ( 9 FDA reports)
DRY MOUTH ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
INTRAOCULAR LENS IMPLANT ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
TREMOR ( 9 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DRY EYE ( 8 FDA reports)
EAR HAEMORRHAGE ( 8 FDA reports)
HAEMATOCHEZIA ( 8 FDA reports)
HIGH FREQUENCY ABLATION ( 8 FDA reports)
MASTOIDITIS ( 8 FDA reports)
MEDICATION ERROR ( 8 FDA reports)
MIOSIS ( 8 FDA reports)
MYOPIA ( 8 FDA reports)
NEUROPATHY PERIPHERAL ( 8 FDA reports)
OTITIS MEDIA ( 8 FDA reports)
BONE PAIN ( 7 FDA reports)
DEATH ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
EYE INFLAMMATION ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 7 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 7 FDA reports)
BLINDNESS UNILATERAL ( 6 FDA reports)
CATHETER PLACEMENT ( 6 FDA reports)
CONJUNCTIVITIS ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
IMPAIRED DRIVING ABILITY ( 6 FDA reports)
LIP SWELLING ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BONE SWELLING ( 5 FDA reports)
DIVERTICULITIS ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
LACERATION ( 5 FDA reports)
LENTIGO ( 5 FDA reports)
MALAISE ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
SEBORRHOEIC KERATOSIS ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HEART RATE IRREGULAR ( 4 FDA reports)
HYPERAEMIA ( 4 FDA reports)
HYSTERECTOMY ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PARAESTHESIA ORAL ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
SKIN HAEMORRHAGE ( 4 FDA reports)
SPONDYLOLISTHESIS ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
STRESS FRACTURE ( 4 FDA reports)
SUDDEN VISUAL LOSS ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CHORIORETINAL DISORDER ( 3 FDA reports)
CHOROIDAL DETACHMENT ( 3 FDA reports)
COUGH ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
EXPIRED DRUG ADMINISTERED ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
EYE OPERATION COMPLICATION ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
HYPOTONY OF EYE ( 3 FDA reports)
INJECTION SITE HAEMORRHAGE ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
OPTIC NERVE DISORDER ( 3 FDA reports)
OSTEITIS DEFORMANS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PRURITUS GENERALISED ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PUPILLARY DISORDER ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RETINAL VEIN THROMBOSIS ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
TERMINAL INSOMNIA ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
AGEUSIA ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BIOPSY ( 2 FDA reports)
BIOPSY BONE ABNORMAL ( 2 FDA reports)
BLEPHAROPACHYNSIS ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORNEAL ABRASION ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CRYING ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
EXPOSED BONE IN JAW ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
EYELID IRRITATION ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE ABNORMAL ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
IMPLANT SITE SWELLING ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INSTILLATION SITE IRRITATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
IRITIS ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JOINT DESTRUCTION ( 2 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PERICARDITIS CONSTRICTIVE ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 2 FDA reports)
PRODUCT LABEL CONFUSION ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL DISORDER ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCLERAL DISORDER ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SCROTAL OEDEMA ( 2 FDA reports)
SOFT TISSUE ATROPHY ( 2 FDA reports)
SOFT TISSUE INJURY ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TEARFULNESS ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
COMA ( 1 FDA reports)
CONJUNCTIVAL FOLLICLES ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COR PULMONALE CHRONIC ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CORNEAL SCAR ( 1 FDA reports)
CORNEAL STAPHYLOMA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
EYELID EXFOLIATION ( 1 FDA reports)
EYELID FOLLICULITIS ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID SENSORY DISORDER ( 1 FDA reports)
EYELID SKIN DRYNESS ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLARE ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS DISORDER ( 1 FDA reports)
IRIS HYPERPIGMENTATION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MELANOSIS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NORMAL TENSION GLAUCOMA ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPTIC NERVE CUP/DISC RATIO INCREASED ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN OPERATION ( 1 FDA reports)
OVARIAN REPAIR ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PLATELET TRANSFUSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUPILLARY DEFORMITY ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCLERAL HYPERAEMIA ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS POLYP ( 1 FDA reports)
SINUSITIS BACTERIAL ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN SENSITISATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
TESTICULAR FAILURE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITREOUS LOSS ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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