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

VOMITING ( 20 FDA reports)
NAUSEA ( 17 FDA reports)
ANAEMIA ( 14 FDA reports)
ASTHENIA ( 14 FDA reports)
ARTHRALGIA ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
DISSEMINATED TUBERCULOSIS ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
HEADACHE ( 11 FDA reports)
LYMPHADENITIS ( 11 FDA reports)
BACK PAIN ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
ERYTHEMA ( 10 FDA reports)
RASH ( 10 FDA reports)
PNEUMONIA ( 9 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
GASTRITIS ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
INTENTIONAL OVERDOSE ( 8 FDA reports)
BRONCHITIS ( 7 FDA reports)
DEATH ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
INSOMNIA ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PALLOR ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CHILLS ( 6 FDA reports)
COUGH ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
INFLAMMATION ( 6 FDA reports)
MENINGITIS ASEPTIC ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
OSTEOARTHRITIS ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
TREMOR ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BURSITIS ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
GLOSSODYNIA ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
HIP FRACTURE ( 5 FDA reports)
HYPERAESTHESIA ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MUSCULOSKELETAL DISORDER ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
PACHYMENINGITIS ( 5 FDA reports)
PAIN ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PELVIC FRACTURE ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RHEUMATOID ARTHRITIS ( 5 FDA reports)
SKIN MASS ( 5 FDA reports)
SWELLING ( 5 FDA reports)
TONGUE DISORDER ( 5 FDA reports)
TUBERCULOSIS ( 5 FDA reports)
VENOUS INSUFFICIENCY ( 5 FDA reports)
BODY HEIGHT DECREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
COLON NEOPLASM ( 4 FDA reports)
COMA ( 4 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 4 FDA reports)
FALL ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MUSCULOSKELETAL DEFORMITY ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
ASTHMATIC CRISIS ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
ENDOMETRIAL CANCER ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NARCOTIC INTOXICATION ( 3 FDA reports)
NO THERAPEUTIC RESPONSE ( 3 FDA reports)
OEDEMA MUCOSAL ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
SCIATICA ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
ARTHRITIS SALMONELLA ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
COAGULATION FACTOR DECREASED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GASTRIC LAVAGE ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE RASH ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LIPOMA ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OCCULT BLOOD ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PULMONARY TUBERCULOSIS ( 2 FDA reports)
PUSTULAR PSORIASIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TENDONITIS ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS INFECTIVE ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPIRATION BRONCHIAL ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
CONJUNCTIVAL EROSION ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
EXTRAPULMONARY TUBERCULOSIS ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTRACRANIAL HYPOTENSION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LATENT TUBERCULOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NODULE ON EXTREMITY ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRIGEMINAL NERVE DISORDER ( 1 FDA reports)
TUBERCULOUS PLEURISY ( 1 FDA reports)
TYPE I HYPERSENSITIVITY ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL ODOUR ( 1 FDA reports)

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