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

ARTHRALGIA ( 25 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
BACK PAIN ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
HEADACHE ( 9 FDA reports)
INFLUENZA LIKE ILLNESS ( 9 FDA reports)
PAIN ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
DYSPNOEA ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
FLATULENCE ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
ALOPECIA ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
CALCIUM DEFICIENCY ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HYPOPNOEA ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
MAGNESIUM DEFICIENCY ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NON-CARDIAC CHEST PAIN ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THYROID NEOPLASM ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VITAMIN D DECREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BURSITIS ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AUTONOMIC NEUROPATHY ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BURNOUT SYNDROME ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH ( 2 FDA reports)
TENSION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FALL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RADIUS FRACTURE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SCLERITIS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TEETHING ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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