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

OSTEONECROSIS OF JAW ( 56 FDA reports)
PAIN ( 54 FDA reports)
PAIN IN EXTREMITY ( 54 FDA reports)
ANXIETY ( 52 FDA reports)
URINARY TRACT INFECTION ( 51 FDA reports)
BACK PAIN ( 50 FDA reports)
BONE DISORDER ( 49 FDA reports)
SPINAL OSTEOARTHRITIS ( 42 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 40 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 39 FDA reports)
CHEST PAIN ( 38 FDA reports)
CONSTIPATION ( 37 FDA reports)
FALL ( 35 FDA reports)
METASTASES TO BONE ( 35 FDA reports)
ARTHRITIS ( 32 FDA reports)
DEPRESSION ( 32 FDA reports)
BRONCHITIS ( 31 FDA reports)
OSTEOPENIA ( 31 FDA reports)
CHILLS ( 29 FDA reports)
HAEMORRHOIDS ( 29 FDA reports)
OEDEMA PERIPHERAL ( 29 FDA reports)
PAIN IN JAW ( 29 FDA reports)
ANAEMIA ( 28 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 28 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 28 FDA reports)
LUMBAR SPINAL STENOSIS ( 28 FDA reports)
BONE LESION ( 27 FDA reports)
NAUSEA ( 26 FDA reports)
ORAL PAIN ( 26 FDA reports)
OSTEOARTHRITIS ( 26 FDA reports)
MICTURITION URGENCY ( 25 FDA reports)
MUSCLE SPASMS ( 25 FDA reports)
NECK PAIN ( 25 FDA reports)
NEUROPATHY PERIPHERAL ( 25 FDA reports)
DYSURIA ( 24 FDA reports)
POLLAKIURIA ( 24 FDA reports)
DYSPEPSIA ( 23 FDA reports)
HEADACHE ( 23 FDA reports)
INJURY ( 23 FDA reports)
NEOPLASM MALIGNANT ( 23 FDA reports)
PNEUMONIA ( 23 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 22 FDA reports)
DECREASED INTEREST ( 22 FDA reports)
DYSPNOEA EXERTIONAL ( 22 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 22 FDA reports)
HYPERLIPIDAEMIA ( 22 FDA reports)
ATRIAL FIBRILLATION ( 21 FDA reports)
CARDIOMEGALY ( 21 FDA reports)
CEREBROVASCULAR ACCIDENT ( 21 FDA reports)
CHOLELITHIASIS ( 21 FDA reports)
DEVICE MALFUNCTION ( 21 FDA reports)
DYSPHAGIA ( 21 FDA reports)
LYMPHADENOPATHY ( 21 FDA reports)
SINUS DISORDER ( 21 FDA reports)
SUICIDAL IDEATION ( 21 FDA reports)
SWELLING ( 21 FDA reports)
VISION BLURRED ( 21 FDA reports)
ABDOMINAL PAIN UPPER ( 20 FDA reports)
AMNESIA ( 20 FDA reports)
DEEP VEIN THROMBOSIS ( 19 FDA reports)
EAR CONGESTION ( 19 FDA reports)
GINGIVAL ERYTHEMA ( 19 FDA reports)
HIATUS HERNIA ( 19 FDA reports)
NODULE ( 19 FDA reports)
ORAL INFECTION ( 19 FDA reports)
SEPSIS ( 19 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
ACUTE CORONARY SYNDROME ( 18 FDA reports)
ARTHRALGIA ( 18 FDA reports)
HUMERUS FRACTURE ( 18 FDA reports)
METASTASES TO LIVER ( 18 FDA reports)
METASTASES TO SPINE ( 18 FDA reports)
METASTASES TO THORAX ( 18 FDA reports)
PULMONARY CONGESTION ( 18 FDA reports)
URINARY RETENTION ( 18 FDA reports)
VASCULAR ANOMALY ( 18 FDA reports)
DECREASED APPETITE ( 17 FDA reports)
HEPATIC CYST ( 17 FDA reports)
LUNG NEOPLASM ( 17 FDA reports)
LYMPHOEDEMA ( 17 FDA reports)
STRESS ( 17 FDA reports)
BLOOD CALCIUM INCREASED ( 16 FDA reports)
DENTAL CARIES ( 16 FDA reports)
EOSINOPHIL COUNT INCREASED ( 16 FDA reports)
HAEMATOCRIT INCREASED ( 16 FDA reports)
LACRIMATION INCREASED ( 16 FDA reports)
LUNG DISORDER ( 16 FDA reports)
MENISCUS LESION ( 16 FDA reports)
PYREXIA ( 16 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 16 FDA reports)
URINARY INCONTINENCE ( 16 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 16 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 15 FDA reports)
DIZZINESS ( 15 FDA reports)
DYSPNOEA ( 15 FDA reports)
FATIGUE ( 15 FDA reports)
HOT FLUSH ( 15 FDA reports)
JAW OPERATION ( 15 FDA reports)
LIBIDO DECREASED ( 15 FDA reports)
SLEEP DISORDER ( 15 FDA reports)
VULVOVAGINAL DRYNESS ( 15 FDA reports)
ASTHENIA ( 14 FDA reports)
BLOOD CORTISOL ABNORMAL ( 14 FDA reports)
BONE PAIN ( 14 FDA reports)
COUGH ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
EYE PRURITUS ( 14 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 14 FDA reports)
FLANK PAIN ( 14 FDA reports)
OSTEOPOROSIS ( 14 FDA reports)
ADJUSTMENT DISORDER ( 13 FDA reports)
ALOPECIA ( 13 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 13 FDA reports)
HYPERHIDROSIS ( 13 FDA reports)
INFECTED SEBACEOUS CYST ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
MENTAL DISORDER ( 13 FDA reports)
NEOPLASM PROGRESSION ( 13 FDA reports)
APNOEA ( 12 FDA reports)
ARTHROPATHY ( 12 FDA reports)
ATELECTASIS ( 12 FDA reports)
BRONCHIAL SECRETION RETENTION ( 12 FDA reports)
BRONCHITIS CHRONIC ( 12 FDA reports)
CARDIOMYOPATHY ( 12 FDA reports)
CEREBRAL ATROPHY ( 12 FDA reports)
CERVICAL CORD COMPRESSION ( 12 FDA reports)
CHONDROMALACIA ( 12 FDA reports)
CONGO-CRIMEAN HAEMORRHAGIC FEVER ( 12 FDA reports)
CONNECTIVE TISSUE DISORDER ( 12 FDA reports)
DENTAL PULP DISORDER ( 12 FDA reports)
DIPLOPIA ( 12 FDA reports)
EJECTION FRACTION DECREASED ( 12 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 12 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 12 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 12 FDA reports)
EMOTIONAL DISTRESS ( 12 FDA reports)
ENCEPHALOPATHY ( 12 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 12 FDA reports)
HAEMOPTYSIS ( 12 FDA reports)
HYPOAESTHESIA ( 12 FDA reports)
ILEUS ( 12 FDA reports)
INFLAMMATION ( 12 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 12 FDA reports)
KYPHOSIS ( 12 FDA reports)
LEFT ATRIAL DILATATION ( 12 FDA reports)
LUDWIG ANGINA ( 12 FDA reports)
LUNG CONSOLIDATION ( 12 FDA reports)
LUNG INFILTRATION ( 12 FDA reports)
MASTICATION DISORDER ( 12 FDA reports)
MULTIPLE MYELOMA ( 12 FDA reports)
MUSCULOSKELETAL PAIN ( 12 FDA reports)
MYASTHENIA GRAVIS ( 12 FDA reports)
NEUTROPENIC SEPSIS ( 12 FDA reports)
OSTEOMYELITIS ( 12 FDA reports)
OSTEOSCLEROSIS ( 12 FDA reports)
OVERDOSE ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
PULMONARY HYPERTENSION ( 12 FDA reports)
RADICULOPATHY ( 12 FDA reports)
SENSITIVITY OF TEETH ( 12 FDA reports)
SPINAL COMPRESSION FRACTURE ( 12 FDA reports)
SPINAL FUSION ACQUIRED ( 12 FDA reports)
SPUTUM DISCOLOURED ( 12 FDA reports)
SUBCUTANEOUS NODULE ( 12 FDA reports)
TOOTH FRACTURE ( 12 FDA reports)
UNRESPONSIVE TO STIMULI ( 12 FDA reports)
UTERINE LEIOMYOMA ( 12 FDA reports)
VENOUS THROMBOSIS ( 12 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 12 FDA reports)
VENTRICULAR TACHYCARDIA ( 12 FDA reports)
ASTHMA ( 11 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 11 FDA reports)
FOLLICULITIS ( 11 FDA reports)
JOINT SWELLING ( 11 FDA reports)
NEPHROLITHIASIS ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
PARAESTHESIA ( 11 FDA reports)
RASH ( 11 FDA reports)
RECTAL HAEMORRHAGE ( 11 FDA reports)
RENAL FAILURE CHRONIC ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
ABSCESS DRAINAGE ( 10 FDA reports)
ADNEXA UTERI MASS ( 10 FDA reports)
ANGIOEDEMA ( 10 FDA reports)
ATROPHIC VULVOVAGINITIS ( 10 FDA reports)
BIOPSY TONGUE ABNORMAL ( 10 FDA reports)
BONE DEBRIDEMENT ( 10 FDA reports)
CEREBRAL ISCHAEMIA ( 10 FDA reports)
COITAL BLEEDING ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
DEFORMITY ( 10 FDA reports)
DERMATITIS ATOPIC ( 10 FDA reports)
ECZEMA ( 10 FDA reports)
EXOSTOSIS ( 10 FDA reports)
FOOT DEFORMITY ( 10 FDA reports)
FOREIGN BODY IN EYE ( 10 FDA reports)
GINGIVAL SWELLING ( 10 FDA reports)
GINGIVAL ULCERATION ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
HYPOPHAGIA ( 10 FDA reports)
HYPOTHYROIDISM ( 10 FDA reports)
KNEE OPERATION ( 10 FDA reports)
LEUKOCYTOSIS ( 10 FDA reports)
LIFE EXPECTANCY SHORTENED ( 10 FDA reports)
MONONUCLEOSIS SYNDROME ( 10 FDA reports)
OEDEMA MOUTH ( 10 FDA reports)
ONYCHOMYCOSIS ( 10 FDA reports)
PERIODONTITIS ( 10 FDA reports)
POLYP ( 10 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 10 FDA reports)
RHINITIS ( 10 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 10 FDA reports)
SCIATICA ( 10 FDA reports)
SKIN DISORDER ( 10 FDA reports)
SOFT TISSUE INFECTION ( 10 FDA reports)
SUBCUTANEOUS ABSCESS ( 10 FDA reports)
SWOLLEN TONGUE ( 10 FDA reports)
TENDON INJURY ( 10 FDA reports)
TOOTH ABSCESS ( 10 FDA reports)
TOOTH EXTRACTION ( 10 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 10 FDA reports)
UTERINE ENLARGEMENT ( 10 FDA reports)
UTERINE POLYP ( 10 FDA reports)
VAGINAL HAEMORRHAGE ( 10 FDA reports)
ACETABULUM FRACTURE ( 9 FDA reports)
ANHEDONIA ( 9 FDA reports)
ARRHYTHMIA ( 9 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 9 FDA reports)
BACTERIAL TEST POSITIVE ( 9 FDA reports)
BIOPSY BONE ( 9 FDA reports)
BONE DENSITY DECREASED ( 9 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 9 FDA reports)
BONE FRAGMENTATION ( 9 FDA reports)
BONE TRIMMING ( 9 FDA reports)
CANDIDIASIS ( 9 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 9 FDA reports)
CARDIAC MURMUR ( 9 FDA reports)
CARPAL TUNNEL SYNDROME ( 9 FDA reports)
CHRONIC SINUSITIS ( 9 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 9 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 9 FDA reports)
CRANIAL NERVE DISORDER ( 9 FDA reports)
CYST ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DENTAL CARE ( 9 FDA reports)
DISABILITY ( 9 FDA reports)
DIVERTICULUM INTESTINAL ( 9 FDA reports)
EAR PAIN ( 9 FDA reports)
EMOTIONAL DISORDER ( 9 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 9 FDA reports)
FACET JOINT SYNDROME ( 9 FDA reports)
FLUID OVERLOAD ( 9 FDA reports)
FOREIGN BODY ( 9 FDA reports)
GINGIVAL INFECTION ( 9 FDA reports)
GINGIVAL PAIN ( 9 FDA reports)
GOITRE ( 9 FDA reports)
HAEMATOMA ( 9 FDA reports)
HAEMATURIA ( 9 FDA reports)
HEAD INJURY ( 9 FDA reports)
HEPATIC STEATOSIS ( 9 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 9 FDA reports)
HYPERMETABOLISM ( 9 FDA reports)
HYPOAESTHESIA ORAL ( 9 FDA reports)
IMPAIRED HEALING ( 9 FDA reports)
JAW DISORDER ( 9 FDA reports)
JOINT INJURY ( 9 FDA reports)
KIDNEY INFECTION ( 9 FDA reports)
LIGAMENT INJURY ( 9 FDA reports)
LOCAL SWELLING ( 9 FDA reports)
LOOSE TOOTH ( 9 FDA reports)
MACROGLOSSIA ( 9 FDA reports)
MASS ( 9 FDA reports)
MENISCUS REMOVAL ( 9 FDA reports)
MITRAL VALVE PROLAPSE ( 9 FDA reports)
MOUTH HAEMORRHAGE ( 9 FDA reports)
MUCOSAL EROSION ( 9 FDA reports)
MUMPS ( 9 FDA reports)
NASAL MUCOSAL DISORDER ( 9 FDA reports)
NECK INJURY ( 9 FDA reports)
ORAL DISCOMFORT ( 9 FDA reports)
OSTEITIS ( 9 FDA reports)
OSTEOMYELITIS CHRONIC ( 9 FDA reports)
PALLOR ( 9 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 9 FDA reports)
PROSTHESIS IMPLANTATION ( 9 FDA reports)
RADIOTHERAPY TO BRAIN ( 9 FDA reports)
RECTAL POLYP ( 9 FDA reports)
RETCHING ( 9 FDA reports)
RUBELLA ( 9 FDA reports)
SCARLET FEVER ( 9 FDA reports)
SCOLIOSIS ( 9 FDA reports)
SEASONAL ALLERGY ( 9 FDA reports)
SKIN PAPILLOMA ( 9 FDA reports)
SLEEP APNOEA SYNDROME ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
TENDONITIS ( 9 FDA reports)
TENOSYNOVITIS STENOSANS ( 9 FDA reports)
TONGUE PARALYSIS ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
TOOTH RESORPTION ( 9 FDA reports)
TOOTHACHE ( 9 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 9 FDA reports)
VITAMIN D DECREASED ( 9 FDA reports)
VOMITING ( 9 FDA reports)
WOUND DEHISCENCE ( 9 FDA reports)
CARTILAGE ATROPHY ( 8 FDA reports)
COLONOSCOPY ABNORMAL ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
GASTROENTERITIS ( 8 FDA reports)
GROIN PAIN ( 8 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 8 FDA reports)
LYMPHOMA ( 8 FDA reports)
MALAISE ( 8 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 8 FDA reports)
NIGHT SWEATS ( 8 FDA reports)
PETECHIAE ( 8 FDA reports)
RENAL CANCER ( 8 FDA reports)
ROTATOR CUFF SYNDROME ( 8 FDA reports)
SEQUESTRECTOMY ( 8 FDA reports)
TOOTH INFECTION ( 8 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
BLADDER DISORDER ( 7 FDA reports)
CERUMEN IMPACTION ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
MUSCLE STRAIN ( 7 FDA reports)
RADICULITIS ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
SPONDYLOLISTHESIS ( 7 FDA reports)
BONE LOSS ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
GASTRIC ULCER ( 6 FDA reports)
LIGAMENT RUPTURE ( 6 FDA reports)
MEDICAL DEVICE REMOVAL ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
NEUROGENIC BLADDER ( 6 FDA reports)
OCULAR HYPERAEMIA ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
RESIDUAL URINE VOLUME ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BREAST CANCER ( 5 FDA reports)
CATARACT ( 5 FDA reports)
CORNEAL ABRASION ( 5 FDA reports)
INFECTED DERMAL CYST ( 5 FDA reports)
LUNG NEOPLASM MALIGNANT ( 5 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 5 FDA reports)
OBESITY ( 5 FDA reports)
PHARYNGITIS ( 5 FDA reports)
RADIOTHERAPY ( 5 FDA reports)
RETINAL TEAR ( 5 FDA reports)
BARTHOLIN'S CYST REMOVAL ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
COLONOSCOPY ( 4 FDA reports)
DEATH ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
FISTULA ( 4 FDA reports)
LYMPHADENECTOMY ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
BIOPSY ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST LUMP REMOVAL ( 3 FDA reports)
BREAST SWELLING ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CONJUNCTIVITIS VIRAL ( 3 FDA reports)
DENTAL FISTULA ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
SINUS HEADACHE ( 3 FDA reports)
TRANSFUSION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COLITIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
LACTOSE INTOLERANCE ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENIERE'S DISEASE ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
METAMORPHOPSIA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PURULENCE ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SINUSITIS FUNGAL ( 2 FDA reports)
SPIDER VEIN ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THROMBOSIS IN DEVICE ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE ( 1 FDA reports)
BONE SCAN ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BUNION OPERATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHONDROSIS ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FOOT OPERATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KERATOMILEUSIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NARCOLEPSY ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLACENTAL INFARCTION ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POLYPECTOMY ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSYCHOTHERAPY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TOE OPERATION ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UMBILICAL CORD ABNORMALITY ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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