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

HYPERTENSION ( 13 FDA reports)
PRE-ECLAMPSIA ( 7 FDA reports)
PROTEINURIA ( 7 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
DIZZINESS ( 5 FDA reports)
FALL ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ARTHRALGIA ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
RHEUMATOID ARTHRITIS ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
FINGER DEFORMITY ( 3 FDA reports)
FOOT OPERATION ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INTESTINAL POLYP ( 3 FDA reports)
JOINT INJURY ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
APNOEA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
EYELID INJURY ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
MULTIPLE FRACTURES ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYING ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HIP DYSPLASIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LACK OF SPONTANEOUS SPEECH ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LUMBAR HERNIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
POLYP ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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