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

APPLICATION SITE IRRITATION ( 165 FDA reports)
BURNING SENSATION ( 138 FDA reports)
APPLICATION SITE PAIN ( 84 FDA reports)
PAIN ( 84 FDA reports)
DRUG INEFFECTIVE ( 59 FDA reports)
ERYTHEMA ( 45 FDA reports)
APPLICATION SITE ERYTHEMA ( 43 FDA reports)
PRURITUS ( 41 FDA reports)
RASH ( 40 FDA reports)
HYPERSENSITIVITY ( 39 FDA reports)
DERMATITIS CONTACT ( 32 FDA reports)
SKIN IRRITATION ( 25 FDA reports)
CRYING ( 22 FDA reports)
BLISTER ( 20 FDA reports)
APPLICATION SITE PRURITUS ( 19 FDA reports)
SWELLING ( 19 FDA reports)
SCREAMING ( 16 FDA reports)
INFECTION ( 13 FDA reports)
THERMAL BURN ( 13 FDA reports)
DRUG ADMINISTRATION ERROR ( 12 FDA reports)
PNEUMONIA ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
CHEILITIS ( 9 FDA reports)
DISCOMFORT ( 9 FDA reports)
LIP SWELLING ( 9 FDA reports)
SKIN BURNING SENSATION ( 9 FDA reports)
APPLICATION SITE REACTION ( 8 FDA reports)
DERMATITIS ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
FUNGAL INFECTION ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
APPLICATION SITE RASH ( 7 FDA reports)
APPLICATION SITE SWELLING ( 7 FDA reports)
APPLICATION SITE VESICLES ( 7 FDA reports)
DEFORMITY ( 7 FDA reports)
FALL ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
WOUND COMPLICATION ( 7 FDA reports)
ACTINOMYCOSIS ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
APPLICATION SITE INFLAMMATION ( 6 FDA reports)
BASAL CELL CARCINOMA ( 6 FDA reports)
BONE DISORDER ( 6 FDA reports)
BONE EROSION ( 6 FDA reports)
BONE LESION ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
COLONIC POLYP ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
CYSTITIS NONINFECTIVE ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
ESSENTIAL HYPERTENSION ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HYPOTHYROIDISM ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
MENINGIOMA ( 6 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 6 FDA reports)
NASAL DISCOMFORT ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
NEOPLASM MALIGNANT ( 6 FDA reports)
OSTEOARTHRITIS ( 6 FDA reports)
OSTEONECROSIS OF JAW ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PANIC ATTACK ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
POLYP ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
RENAL CYST ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
SEBORRHOEIC KERATOSIS ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
SQUAMOUS CELL CARCINOMA ( 6 FDA reports)
SWELLING FACE ( 6 FDA reports)
TENDONITIS ( 6 FDA reports)
TONGUE DISORDER ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
APPLICATION SITE DISCHARGE ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
COLITIS ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GASTROINTESTINAL TOXICITY ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
MALNUTRITION ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
APPLICATION SITE EXFOLIATION ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BLEPHARITIS ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MALIGNANT HYPERTENSION ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NONSPECIFIC REACTION ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
RASH VESICULAR ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
ROSACEA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN BACTERIAL INFECTION ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ACUTE LUNG INJURY ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
APPLICATION SITE BURN ( 3 FDA reports)
APPLICATION SITE DISCOMFORT ( 3 FDA reports)
APPLICATION SITE PARAESTHESIA ( 3 FDA reports)
APPLICATION SITE SCAR ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INJURY ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
ISCHAEMIA ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
TOE AMPUTATION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 3 FDA reports)
WOUND ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
APPLICATION SITE ABSCESS ( 2 FDA reports)
APPLICATION SITE DISCOLOURATION ( 2 FDA reports)
APPLICATION SITE ECZEMA ( 2 FDA reports)
APPLICATION SITE INFECTION ( 2 FDA reports)
APPLICATION SITE URTICARIA ( 2 FDA reports)
APPLICATION SITE WARMTH ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
FURUNCLE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEAR DROWNING ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PEPTIC ULCER ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
RADIATION ASSOCIATED PAIN ( 2 FDA reports)
RETINAL ARTERY THROMBOSIS ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SCAB ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPONDYLOARTHROPATHY ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ULCER ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
VAGINAL PAIN ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE BLEEDING ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
APPLICATION SITE HYPERAESTHESIA ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE ULCER ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CROSS SENSITIVITY REACTION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP PRURITUS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PENILE ERYTHEMA ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RETINOPATHY HAEMORRHAGIC ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VAGINAL SWELLING ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VESTIBULAR FUNCTION TEST ABNORMAL ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)

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