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

CHILLS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
FALL ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COMA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG LOBECTOMY ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENSION HEADACHE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)

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