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

DRUG DOSE OMISSION ( 9 FDA reports)
ANXIETY ( 8 FDA reports)
MALAISE ( 8 FDA reports)
DIZZINESS ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
BREAST CANCER ( 5 FDA reports)
DERMATITIS ALLERGIC ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
RECTAL ABSCESS ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
VOMITING ( 5 FDA reports)
FALL ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
PAIN ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
AGEUSIA ( 2 FDA reports)
ANGER ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BREAST CYST ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VICTIM OF CRIME ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING OF DESPAIR ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
MALIGNANT NEOPLASM OF SPINAL CORD ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PREGNANCY AFTER POST COITAL CONTRACEPTION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC PAIN ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RADIOTHERAPY ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SEXUAL OFFENCE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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