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

PAIN ( 15 FDA reports)
DYSPNOEA ( 14 FDA reports)
MALAISE ( 13 FDA reports)
DIZZINESS ( 11 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
PRURITUS ( 9 FDA reports)
HEADACHE ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
DIARRHOEA ( 7 FDA reports)
COUGH ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ARTHRITIS ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
EYE OEDEMA ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
FUNGAL RASH ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
RALES ( 4 FDA reports)
RASH ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CRYOTHERAPY ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
EXCORIATION ( 3 FDA reports)
FALL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTERTRIGO ( 3 FDA reports)
LICHEN PLANUS ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
RASH MORBILLIFORM ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SEBACEOUS HYPERPLASIA ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
APHAGIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COUNTERFEIT DRUG ADMINISTERED ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
SCAR ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRESS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URINE ODOUR ABNORMAL ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLONOSCOPY ABNORMAL ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL INFLAMMATION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRODUCT BLISTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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